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	<id>https://www.iec.wiki/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=EMC</id>
	<title>认证百科 - 用户贡献 [zh-cn]</title>
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	<link rel="alternate" type="text/html" href="https://www.iec.wiki/%E7%89%B9%E6%AE%8A:%E7%94%A8%E6%88%B7%E8%B4%A1%E7%8C%AE/EMC"/>
	<updated>2026-07-31T04:35:14Z</updated>
	<subtitle>用户贡献</subtitle>
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	<entry>
		<id>https://www.iec.wiki/index.php?title=FCC_ID_Search&amp;diff=346</id>
		<title>FCC ID Search</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=FCC_ID_Search&amp;diff=346"/>
		<updated>2019-09-22T17:01:02Z</updated>

		<summary type="html">&lt;p&gt;EMC：​/* FCC ID 规则 */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==&#039;&#039;&#039;FCC认证中如何确认是否有做过FCC ID认证呢？&#039;&#039;&#039;==&lt;br /&gt;
（1）可以通过查询FRN号码与Grantee Code号码，如果有那么就可能做过FCC ID认证了。&lt;br /&gt;
（2）通过完整的FCC ID号=Grantee Code号码+产品代码进行查询&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;查询企业的FRN号码&#039;&#039;&#039;==&lt;br /&gt;
Applicant’s FCC Registration Number (FRN) ，此为政府给予企业的身份识别号，可在FCC官方网站免费申请，申请后由网站自动生成给企业。打开 apps.fcc.gov/coresWeb/simpleSearch.do 网页，并在如下图片的黄色框框里面输入企业全称。&lt;br /&gt;
[[File:FCC Registration Number - FRN.jpg|832x421px]]&lt;br /&gt;
&lt;br /&gt;
如果这个里面查询不到，那么这个企业肯定是没有做过FCC ID认证，至少以这个企业名称，肯定是没有申请过FCC ID。&lt;br /&gt;
&lt;br /&gt;
以Fotorama (Hong Kong) Limited 公司为例子进行查询，如下图所示，这家企业在06/10/2011已经在FCC官方网站注册，那么这个企业很有可能做过FCC认证了，但是不能肯定，做完这一步还不能肯定客户实际做过FCC ID认证，然后进行下一步。&lt;br /&gt;
&lt;br /&gt;
[[File:FCC FRN.jpg|1904x213px]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;查询企业的Grantee Code号码（授权码）&#039;&#039;&#039;==&lt;br /&gt;
对于第一次申请 FCC ID的客户可在申请 FRN号后，申请 Grantee Code(需付费约几十美金，详细以FCC官方为准)，只需申请一次。Grantee Code (3位或5位字母或数值)，每个Grantee Code只代表一间公司，该3位或5位号码由FCC随机提供，并非由客户自定。&lt;br /&gt;
&lt;br /&gt;
在网站 apps.fcc.gov/oetcf/eas/reports/GranteeSearch.cfm 打开页面，输入FCC ID号的前3位或者前5位字母或者横杠代码。例如，以Fotorama (Hong Kong) Limited 公司为例查询，如下图所示厂家的Grantee Code为ZNK。&lt;br /&gt;
&lt;br /&gt;
[[File:Grantee Name - Fotorama Hong Kong - Limited.jpg|1612x229px]]&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;查询企业的做过的FCC ID认证&#039;&#039;&#039;==&lt;br /&gt;
知道了客户的Grantee Code号码（授权码）为ZNK，那么进行最后一步查询。打开网站 apps.fcc.gov/oetcf/eas/reports/GenericSearch.cfm 页面，在红色方框里面输入ZNK，然后点击页面最下面的Start Search.&lt;br /&gt;
&lt;br /&gt;
[[File:Grantee Code Search.jpg|1194x453px]]&lt;br /&gt;
&lt;br /&gt;
然后搜索出来显示，客户已经做了7份报告。分别在2011年三个产品FCC ID认证，2012年2个产品FCC ID认证，2019年分别在06/10，07/01做了3个产品认证，详细如下图所示。&lt;br /&gt;
&lt;br /&gt;
[[File:Grantee Code - ZNK - test report.jpg|1440x407px]]&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;FCC ID 规则&#039;&#039;&#039;==&lt;br /&gt;
FCC ID包括Grantee Code 公司代号(3位或5位字母或数值)，每个Grantee Code只代表一间公司。该3位或5位号码由FCC随机提供，并非由客户自定。一旦申请成功，即成为固定的号码，作为该公司所有申请FCC ID 号码的前3位或5位代号。以及Product code产品的代号(10~12位字母或数值)。所以产品 ID号，前三位或者五位为 Grantee Code，后面由申请商自编(最多 10~12位)，通常用产品型号做自编码，完整的FCC ID最多不能大于15个，当然了，可以少于15个。&lt;br /&gt;
* （1）Grantee Code为三个字符的 Grantee Code始终以字母字符开头，并且不包含数字1和/或0。&lt;br /&gt;
* （2）Grantee Code为五个字符的 Grantee Code始终以数字字符开头，并且不包含数字1和/或0。&lt;br /&gt;
* （3）产品代码可能包含连字符破折号（-）。&lt;br /&gt;
* （4）FCC ID的最大位数不能大于15位。&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=FCC_ID_Search&amp;diff=345</id>
		<title>FCC ID Search</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=FCC_ID_Search&amp;diff=345"/>
		<updated>2019-09-22T16:59:26Z</updated>

		<summary type="html">&lt;p&gt;EMC：​/* FCC ID 规则 */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==&#039;&#039;&#039;FCC认证中如何确认是否有做过FCC ID认证呢？&#039;&#039;&#039;==&lt;br /&gt;
（1）可以通过查询FRN号码与Grantee Code号码，如果有那么就可能做过FCC ID认证了。&lt;br /&gt;
（2）通过完整的FCC ID号=Grantee Code号码+产品代码进行查询&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;查询企业的FRN号码&#039;&#039;&#039;==&lt;br /&gt;
Applicant’s FCC Registration Number (FRN) ，此为政府给予企业的身份识别号，可在FCC官方网站免费申请，申请后由网站自动生成给企业。打开 apps.fcc.gov/coresWeb/simpleSearch.do 网页，并在如下图片的黄色框框里面输入企业全称。&lt;br /&gt;
[[File:FCC Registration Number - FRN.jpg|832x421px]]&lt;br /&gt;
&lt;br /&gt;
如果这个里面查询不到，那么这个企业肯定是没有做过FCC ID认证，至少以这个企业名称，肯定是没有申请过FCC ID。&lt;br /&gt;
&lt;br /&gt;
以Fotorama (Hong Kong) Limited 公司为例子进行查询，如下图所示，这家企业在06/10/2011已经在FCC官方网站注册，那么这个企业很有可能做过FCC认证了，但是不能肯定，做完这一步还不能肯定客户实际做过FCC ID认证，然后进行下一步。&lt;br /&gt;
&lt;br /&gt;
[[File:FCC FRN.jpg|1904x213px]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;查询企业的Grantee Code号码（授权码）&#039;&#039;&#039;==&lt;br /&gt;
对于第一次申请 FCC ID的客户可在申请 FRN号后，申请 Grantee Code(需付费约几十美金，详细以FCC官方为准)，只需申请一次。Grantee Code (3位或5位字母或数值)，每个Grantee Code只代表一间公司，该3位或5位号码由FCC随机提供，并非由客户自定。&lt;br /&gt;
&lt;br /&gt;
在网站 apps.fcc.gov/oetcf/eas/reports/GranteeSearch.cfm 打开页面，输入FCC ID号的前3位或者前5位字母或者横杠代码。例如，以Fotorama (Hong Kong) Limited 公司为例查询，如下图所示厂家的Grantee Code为ZNK。&lt;br /&gt;
&lt;br /&gt;
[[File:Grantee Name - Fotorama Hong Kong - Limited.jpg|1612x229px]]&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;查询企业的做过的FCC ID认证&#039;&#039;&#039;==&lt;br /&gt;
知道了客户的Grantee Code号码（授权码）为ZNK，那么进行最后一步查询。打开网站 apps.fcc.gov/oetcf/eas/reports/GenericSearch.cfm 页面，在红色方框里面输入ZNK，然后点击页面最下面的Start Search.&lt;br /&gt;
&lt;br /&gt;
[[File:Grantee Code Search.jpg|1194x453px]]&lt;br /&gt;
&lt;br /&gt;
然后搜索出来显示，客户已经做了7份报告。分别在2011年三个产品FCC ID认证，2012年2个产品FCC ID认证，2019年分别在06/10，07/01做了3个产品认证，详细如下图所示。&lt;br /&gt;
&lt;br /&gt;
[[File:Grantee Code - ZNK - test report.jpg|1440x407px]]&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;FCC ID 规则&#039;&#039;&#039;==&lt;br /&gt;
FCC ID包括Grantee Code 公司代号(3位或5位字母或数值)，每个Grantee Code只代表一间公司。该3位或5位号码由FCC随机提供，并非由客户自定。一旦申请成功，即成为固定的号码，作为该公司所有申请FCC ID 号码的前3位或5位代号。以及Product code产品的代号(1-14位字母或数值)。所以产品 ID号，前三位或者五位为 Grantee Code，后面由申请商自编(最多 14位)，通常用产品型号做自编码。&lt;br /&gt;
* （1）Grantee Code为三个字符的 Grantee Code始终以字母字符开头，并且不包含数字1和/或0。&lt;br /&gt;
* （2）Grantee Code为五个字符的 Grantee Code始终以数字字符开头，并且不包含数字1和/或0。&lt;br /&gt;
* （3）产品代码可能包含连字符破折号（-）。&lt;br /&gt;
* （4）FCC ID的最大位数不能大于15位。&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=FCC_ID_Search&amp;diff=344</id>
		<title>FCC ID Search</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=FCC_ID_Search&amp;diff=344"/>
		<updated>2019-09-22T16:59:15Z</updated>

		<summary type="html">&lt;p&gt;EMC：​/* 查询企业的做过的认证 */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==&#039;&#039;&#039;FCC认证中如何确认是否有做过FCC ID认证呢？&#039;&#039;&#039;==&lt;br /&gt;
（1）可以通过查询FRN号码与Grantee Code号码，如果有那么就可能做过FCC ID认证了。&lt;br /&gt;
（2）通过完整的FCC ID号=Grantee Code号码+产品代码进行查询&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;查询企业的FRN号码&#039;&#039;&#039;==&lt;br /&gt;
Applicant’s FCC Registration Number (FRN) ，此为政府给予企业的身份识别号，可在FCC官方网站免费申请，申请后由网站自动生成给企业。打开 apps.fcc.gov/coresWeb/simpleSearch.do 网页，并在如下图片的黄色框框里面输入企业全称。&lt;br /&gt;
[[File:FCC Registration Number - FRN.jpg|832x421px]]&lt;br /&gt;
&lt;br /&gt;
如果这个里面查询不到，那么这个企业肯定是没有做过FCC ID认证，至少以这个企业名称，肯定是没有申请过FCC ID。&lt;br /&gt;
&lt;br /&gt;
以Fotorama (Hong Kong) Limited 公司为例子进行查询，如下图所示，这家企业在06/10/2011已经在FCC官方网站注册，那么这个企业很有可能做过FCC认证了，但是不能肯定，做完这一步还不能肯定客户实际做过FCC ID认证，然后进行下一步。&lt;br /&gt;
&lt;br /&gt;
[[File:FCC FRN.jpg|1904x213px]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;查询企业的Grantee Code号码（授权码）&#039;&#039;&#039;==&lt;br /&gt;
对于第一次申请 FCC ID的客户可在申请 FRN号后，申请 Grantee Code(需付费约几十美金，详细以FCC官方为准)，只需申请一次。Grantee Code (3位或5位字母或数值)，每个Grantee Code只代表一间公司，该3位或5位号码由FCC随机提供，并非由客户自定。&lt;br /&gt;
&lt;br /&gt;
在网站 apps.fcc.gov/oetcf/eas/reports/GranteeSearch.cfm 打开页面，输入FCC ID号的前3位或者前5位字母或者横杠代码。例如，以Fotorama (Hong Kong) Limited 公司为例查询，如下图所示厂家的Grantee Code为ZNK。&lt;br /&gt;
&lt;br /&gt;
[[File:Grantee Name - Fotorama Hong Kong - Limited.jpg|1612x229px]]&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;查询企业的做过的FCC ID认证&#039;&#039;&#039;==&lt;br /&gt;
知道了客户的Grantee Code号码（授权码）为ZNK，那么进行最后一步查询。打开网站 apps.fcc.gov/oetcf/eas/reports/GenericSearch.cfm 页面，在红色方框里面输入ZNK，然后点击页面最下面的Start Search.&lt;br /&gt;
&lt;br /&gt;
[[File:Grantee Code Search.jpg|1194x453px]]&lt;br /&gt;
&lt;br /&gt;
然后搜索出来显示，客户已经做了7份报告。分别在2011年三个产品FCC ID认证，2012年2个产品FCC ID认证，2019年分别在06/10，07/01做了3个产品认证，详细如下图所示。&lt;br /&gt;
&lt;br /&gt;
[[File:Grantee Code - ZNK - test report.jpg|1440x407px]]&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;FCC ID 规则&#039;&#039;&#039;==&lt;br /&gt;
FCC ID包括Grantee Code 公司代号(3位或5位字母或数值)，每个Grantee Code只代表一间公司。该3位或5位号码由FCC随机提供，并非由客户自定。一旦申请成功，即成为固定的号码，作为该公司所有申请FCC ID 号码的前3位或5位代号。以及Product code产品的代号(1-14位字母或数值)。所以产品 ID号，前三位或者五位为 Grantee Code，后面由申请商自编(最多 14位)，通常用产品型号做自编码。&lt;br /&gt;
（1）Grantee Code为三个字符的 Grantee Code始终以字母字符开头，并且不包含数字1和/或0。&lt;br /&gt;
（2）Grantee Code为五个字符的 Grantee Code始终以数字字符开头，并且不包含数字1和/或0。&lt;br /&gt;
（3）产品代码可能包含连字符破折号（-）。&lt;br /&gt;
（4）FCC ID的最大位数不能大于15位。&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=FCC_ID_Search&amp;diff=343</id>
		<title>FCC ID Search</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=FCC_ID_Search&amp;diff=343"/>
		<updated>2019-09-22T16:58:53Z</updated>

		<summary type="html">&lt;p&gt;EMC：​/* FCC认证中如何确认是否有做过FCC ID认证呢？ */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==&#039;&#039;&#039;FCC认证中如何确认是否有做过FCC ID认证呢？&#039;&#039;&#039;==&lt;br /&gt;
（1）可以通过查询FRN号码与Grantee Code号码，如果有那么就可能做过FCC ID认证了。&lt;br /&gt;
（2）通过完整的FCC ID号=Grantee Code号码+产品代码进行查询&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;查询企业的FRN号码&#039;&#039;&#039;==&lt;br /&gt;
Applicant’s FCC Registration Number (FRN) ，此为政府给予企业的身份识别号，可在FCC官方网站免费申请，申请后由网站自动生成给企业。打开 apps.fcc.gov/coresWeb/simpleSearch.do 网页，并在如下图片的黄色框框里面输入企业全称。&lt;br /&gt;
[[File:FCC Registration Number - FRN.jpg|832x421px]]&lt;br /&gt;
&lt;br /&gt;
如果这个里面查询不到，那么这个企业肯定是没有做过FCC ID认证，至少以这个企业名称，肯定是没有申请过FCC ID。&lt;br /&gt;
&lt;br /&gt;
以Fotorama (Hong Kong) Limited 公司为例子进行查询，如下图所示，这家企业在06/10/2011已经在FCC官方网站注册，那么这个企业很有可能做过FCC认证了，但是不能肯定，做完这一步还不能肯定客户实际做过FCC ID认证，然后进行下一步。&lt;br /&gt;
&lt;br /&gt;
[[File:FCC FRN.jpg|1904x213px]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;查询企业的Grantee Code号码（授权码）&#039;&#039;&#039;==&lt;br /&gt;
对于第一次申请 FCC ID的客户可在申请 FRN号后，申请 Grantee Code(需付费约几十美金，详细以FCC官方为准)，只需申请一次。Grantee Code (3位或5位字母或数值)，每个Grantee Code只代表一间公司，该3位或5位号码由FCC随机提供，并非由客户自定。&lt;br /&gt;
&lt;br /&gt;
在网站 apps.fcc.gov/oetcf/eas/reports/GranteeSearch.cfm 打开页面，输入FCC ID号的前3位或者前5位字母或者横杠代码。例如，以Fotorama (Hong Kong) Limited 公司为例查询，如下图所示厂家的Grantee Code为ZNK。&lt;br /&gt;
&lt;br /&gt;
[[File:Grantee Name - Fotorama Hong Kong - Limited.jpg|1612x229px]]&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;查询企业的做过的认证&#039;&#039;&#039;==&lt;br /&gt;
知道了客户的Grantee Code号码（授权码）为ZNK，那么进行最后一步查询。打开网站 apps.fcc.gov/oetcf/eas/reports/GenericSearch.cfm 页面，在红色方框里面输入ZNK，然后点击页面最下面的Start Search.&lt;br /&gt;
&lt;br /&gt;
[[File:Grantee Code Search.jpg|1194x453px]]&lt;br /&gt;
&lt;br /&gt;
然后搜索出来显示，客户已经做了7份报告。分别在2011年三个产品FCC ID认证，2012年2个产品FCC ID认证，2019年分别在06/10，07/01做了3个产品认证，详细如下图所示。&lt;br /&gt;
&lt;br /&gt;
[[File:Grantee Code - ZNK - test report.jpg|1440x407px]]&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;FCC ID 规则&#039;&#039;&#039;==&lt;br /&gt;
FCC ID包括Grantee Code 公司代号(3位或5位字母或数值)，每个Grantee Code只代表一间公司。该3位或5位号码由FCC随机提供，并非由客户自定。一旦申请成功，即成为固定的号码，作为该公司所有申请FCC ID 号码的前3位或5位代号。以及Product code产品的代号(1-14位字母或数值)。所以产品 ID号，前三位或者五位为 Grantee Code，后面由申请商自编(最多 14位)，通常用产品型号做自编码。&lt;br /&gt;
（1）Grantee Code为三个字符的 Grantee Code始终以字母字符开头，并且不包含数字1和/或0。&lt;br /&gt;
（2）Grantee Code为五个字符的 Grantee Code始终以数字字符开头，并且不包含数字1和/或0。&lt;br /&gt;
（3）产品代码可能包含连字符破折号（-）。&lt;br /&gt;
（4）FCC ID的最大位数不能大于15位。&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=FCC_ID_Search&amp;diff=342</id>
		<title>FCC ID Search</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=FCC_ID_Search&amp;diff=342"/>
		<updated>2019-09-22T16:56:16Z</updated>

		<summary type="html">&lt;p&gt;EMC：​Created page with &amp;quot;==&amp;#039;&amp;#039;&amp;#039;FCC认证中如何确认是否有做过FCC ID认证呢？&amp;#039;&amp;#039;&amp;#039;==   ==&amp;#039;&amp;#039;&amp;#039;查询企业的FRN号码&amp;#039;&amp;#039;&amp;#039;== Applicant’s FCC Registration Number (FRN) ，此为政府给予企...&amp;quot;&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==&#039;&#039;&#039;FCC认证中如何确认是否有做过FCC ID认证呢？&#039;&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;查询企业的FRN号码&#039;&#039;&#039;==&lt;br /&gt;
Applicant’s FCC Registration Number (FRN) ，此为政府给予企业的身份识别号，可在FCC官方网站免费申请，申请后由网站自动生成给企业。打开 apps.fcc.gov/coresWeb/simpleSearch.do 网页，并在如下图片的黄色框框里面输入企业全称。&lt;br /&gt;
[[File:FCC Registration Number - FRN.jpg|832x421px]]&lt;br /&gt;
&lt;br /&gt;
如果这个里面查询不到，那么这个企业肯定是没有做过FCC ID认证，至少以这个企业名称，肯定是没有申请过FCC ID。&lt;br /&gt;
&lt;br /&gt;
以Fotorama (Hong Kong) Limited 公司为例子进行查询，如下图所示，这家企业在06/10/2011已经在FCC官方网站注册，那么这个企业很有可能做过FCC认证了，但是不能肯定，做完这一步还不能肯定客户实际做过FCC ID认证，然后进行下一步。&lt;br /&gt;
&lt;br /&gt;
[[File:FCC FRN.jpg|1904x213px]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;查询企业的Grantee Code号码（授权码）&#039;&#039;&#039;==&lt;br /&gt;
对于第一次申请 FCC ID的客户可在申请 FRN号后，申请 Grantee Code(需付费约几十美金，详细以FCC官方为准)，只需申请一次。Grantee Code (3位或5位字母或数值)，每个Grantee Code只代表一间公司，该3位或5位号码由FCC随机提供，并非由客户自定。&lt;br /&gt;
&lt;br /&gt;
在网站 apps.fcc.gov/oetcf/eas/reports/GranteeSearch.cfm 打开页面，输入FCC ID号的前3位或者前5位字母或者横杠代码。例如，以Fotorama (Hong Kong) Limited 公司为例查询，如下图所示厂家的Grantee Code为ZNK。&lt;br /&gt;
&lt;br /&gt;
[[File:Grantee Name - Fotorama Hong Kong - Limited.jpg|1612x229px]]&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;查询企业的做过的认证&#039;&#039;&#039;==&lt;br /&gt;
知道了客户的Grantee Code号码（授权码）为ZNK，那么进行最后一步查询。打开网站 apps.fcc.gov/oetcf/eas/reports/GenericSearch.cfm 页面，在红色方框里面输入ZNK，然后点击页面最下面的Start Search.&lt;br /&gt;
&lt;br /&gt;
[[File:Grantee Code Search.jpg|1194x453px]]&lt;br /&gt;
&lt;br /&gt;
然后搜索出来显示，客户已经做了7份报告。分别在2011年三个产品FCC ID认证，2012年2个产品FCC ID认证，2019年分别在06/10，07/01做了3个产品认证，详细如下图所示。&lt;br /&gt;
&lt;br /&gt;
[[File:Grantee Code - ZNK - test report.jpg|1440x407px]]&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;FCC ID 规则&#039;&#039;&#039;==&lt;br /&gt;
FCC ID包括Grantee Code 公司代号(3位或5位字母或数值)，每个Grantee Code只代表一间公司。该3位或5位号码由FCC随机提供，并非由客户自定。一旦申请成功，即成为固定的号码，作为该公司所有申请FCC ID 号码的前3位或5位代号。以及Product code产品的代号(1-14位字母或数值)。所以产品 ID号，前三位或者五位为 Grantee Code，后面由申请商自编(最多 14位)，通常用产品型号做自编码。&lt;br /&gt;
（1）Grantee Code为三个字符的 Grantee Code始终以字母字符开头，并且不包含数字1和/或0。&lt;br /&gt;
（2）Grantee Code为五个字符的 Grantee Code始终以数字字符开头，并且不包含数字1和/或0。&lt;br /&gt;
（3）产品代码可能包含连字符破折号（-）。&lt;br /&gt;
（4）FCC ID的最大位数不能大于15位。&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:Grantee_Code_-_ZNK_-_test_report.jpg&amp;diff=341</id>
		<title>文件:Grantee Code - ZNK - test report.jpg</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:Grantee_Code_-_ZNK_-_test_report.jpg&amp;diff=341"/>
		<updated>2019-09-22T16:52:47Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Grantee Code - ZNK - test report&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:Grantee_Code_Search.jpg&amp;diff=340</id>
		<title>文件:Grantee Code Search.jpg</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:Grantee_Code_Search.jpg&amp;diff=340"/>
		<updated>2019-09-22T16:51:53Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Grantee Code Search&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:Grantee_Name_-_Fotorama_Hong_Kong_-_Limited.jpg&amp;diff=339</id>
		<title>文件:Grantee Name - Fotorama Hong Kong - Limited.jpg</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:Grantee_Name_-_Fotorama_Hong_Kong_-_Limited.jpg&amp;diff=339"/>
		<updated>2019-09-22T16:50:44Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Grantee Name - Fotorama Hong Kong - Limited&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:FCC_FRN.jpg&amp;diff=338</id>
		<title>文件:FCC FRN.jpg</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:FCC_FRN.jpg&amp;diff=338"/>
		<updated>2019-09-22T16:48:41Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;FCC FRN&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:FCC_Registration_Number_-_FRN.jpg&amp;diff=337</id>
		<title>文件:FCC Registration Number - FRN.jpg</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:FCC_Registration_Number_-_FRN.jpg&amp;diff=337"/>
		<updated>2019-09-22T16:46:30Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;FCC Registration Number - FRN&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:Search.png&amp;diff=203</id>
		<title>文件:Search.png</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:Search.png&amp;diff=203"/>
		<updated>2019-09-04T18:24:56Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:SRRC.png&amp;diff=202</id>
		<title>文件:SRRC.png</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:SRRC.png&amp;diff=202"/>
		<updated>2019-09-04T18:24:56Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:VCCI-logo.png&amp;diff=201</id>
		<title>文件:VCCI-logo.png</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:VCCI-logo.png&amp;diff=201"/>
		<updated>2019-09-04T18:24:56Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:WIFI-HT20-HT40.png&amp;diff=200</id>
		<title>文件:WIFI-HT20-HT40.png</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:WIFI-HT20-HT40.png&amp;diff=200"/>
		<updated>2019-09-04T18:24:56Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:Nvlap.jpg&amp;diff=199</id>
		<title>文件:Nvlap.jpg</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:Nvlap.jpg&amp;diff=199"/>
		<updated>2019-09-04T18:24:56Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:240px-BT_channels.jpg&amp;diff=198</id>
		<title>文件:240px-BT channels.jpg</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:240px-BT_channels.jpg&amp;diff=198"/>
		<updated>2019-09-04T18:24:56Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:8r8ahkz4mn8cidj1zjzw5mrbn13jqx6.png&amp;diff=197</id>
		<title>文件:8r8ahkz4mn8cidj1zjzw5mrbn13jqx6.png</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:8r8ahkz4mn8cidj1zjzw5mrbn13jqx6.png&amp;diff=197"/>
		<updated>2019-09-04T18:21:37Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:89px-%E5%B9%BF%E6%92%AD%E7%94%B5%E8%A7%86%E8%AE%BE%E5%A4%87%E5%99%A8%E6%9D%90%E5%85%A5%E7%BD%91%E8%AE%A4%E5%AE%9A%E8%AF%81%E4%B9%A6.jpg&amp;diff=196</id>
		<title>文件:89px-广播电视设备器材入网认定证书.jpg</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:89px-%E5%B9%BF%E6%92%AD%E7%94%B5%E8%A7%86%E8%AE%BE%E5%A4%87%E5%99%A8%E6%9D%90%E5%85%A5%E7%BD%91%E8%AE%A4%E5%AE%9A%E8%AF%81%E4%B9%A6.jpg&amp;diff=196"/>
		<updated>2019-09-04T18:21:37Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:102px-NOM.jpg&amp;diff=195</id>
		<title>文件:102px-NOM.jpg</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:102px-NOM.jpg&amp;diff=195"/>
		<updated>2019-09-04T18:21:37Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:BT_channels.jpg&amp;diff=194</id>
		<title>文件:BT channels.jpg</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:BT_channels.jpg&amp;diff=194"/>
		<updated>2019-09-04T18:19:16Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:2.4_GHz_Wi-Fi_channels_802.11b,g_WLAN.png&amp;diff=193</id>
		<title>文件:2.4 GHz Wi-Fi channels 802.11b,g WLAN.png</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E6%96%87%E4%BB%B6:2.4_GHz_Wi-Fi_channels_802.11b,g_WLAN.png&amp;diff=193"/>
		<updated>2019-09-04T18:19:16Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=FCC_ID&amp;diff=64</id>
		<title>FCC ID</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=FCC_ID&amp;diff=64"/>
		<updated>2019-08-26T06:38:33Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==&#039;&#039;&#039;什么是FCC ID？&#039;&#039;&#039;==&lt;br /&gt;
FCC ID是指美国的FCC Certification无线认证，通过认证后会有一串号码，俗称FCC ID认证。&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;FCC标识符&#039;&#039;&#039;==&lt;br /&gt;
FCC ID认证必须在铭牌上面打上已经获得认证的ID号码，例如：FCC ID AAAAAXXXXX，AAAAA 代表5位字符的厂商编码（Grantee Code），XXXXX 由不超过14位的数字、字母、中横杆字符组成，是申请人设备的唯一代码，中横杆-也算一位字符。&lt;br /&gt;
[[文件:FCC.jpg|330x220px|无框]]&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;FCC ID&#039;&#039;&#039;（FCC CERTIFICATION认证证书）认证&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;FCC ID产品包括&#039;&#039;&#039;==&lt;br /&gt;
 无线射频产品，例如BT、Wifi、Zigbee、2.4GHz、5GHz、手机产品、各类遥控器等有意发射产品，均需要符合美国FCC PART 15C标准限值。&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;认证方式&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
（1）产品需通过FCC认可的测试室测试完毕，取得测试报告后。&lt;br /&gt;
&lt;br /&gt;
（2）整理产品的技术资料，包括：产品细节照片、方块图、使用手册等，详细资料可参阅 https://www.emc.wiki/thread-2297-1-1.html 。&lt;br /&gt;
&lt;br /&gt;
（3）再由FCC 认可的NVLAP &amp;amp; A2LA 测试实验室提交给FCC TCB测试室确认所有资料无误（或者直接找TCB），并颁发证书。&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;FCC ID基本申请流程&#039;&#039;&#039;==&lt;br /&gt;
（1）&#039;&#039;&#039;在中国必须要找拥有NVLAP or A2LA美国认可的无线射频实验室申请&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
（3）申请FCC ID = Grantee Code + Product code（申请成功之后将会拥有这串号码）先申请一个 FRN ，用来填写其它的表格。&lt;br /&gt;
&lt;br /&gt;
（3）如果申请人是第一次申请 FCC ID ，就需要申请一个永久性的 Grantee Code 。在等待FCC批准分发给申请人 Grantee Code 的同时，申请人应抓紧时间将设备进行检测。待准备好所有 FCC 要求提交的材料并且检测报告已经完成时， FCC 应该已经批准了 Grantee Code 。申请人用这个 Code 、检测报告和要求的材料在网上完成 FCC Form 731 和 Form 159 。 FCC 收到 Form 159 和汇款后，就开始受理认证的申请。受理结束时， FCC 会将 FCC ID 的 Original Grant 寄给申请人。申请人拿到证书后就可以出售或出口相应产品了。&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;FCC ID认证基本资料&#039;&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
*Applicant’s Product Name ,Model NO., Mailing Address , Phone No.,Fax No., Contact Person &amp;amp; His Title。申请方的名字，产品名，型号，地址，电话，邮件，传真，联系人及其职位。&lt;br /&gt;
&lt;br /&gt;
*For transmitter, the fundamental frequency(Operation within the bands)。针对发射部分，发射的基波频率(最好提供使用的频段)。&lt;br /&gt;
&lt;br /&gt;
*Applicant’s FCC Registration Number (FRN) 申请方的FCC的注册号码FRN（ FCC Registration Number），此为政府给予企业的身份识别号，可在FCC官方网站免费申请，在申请后由网站自动生成给企业，共10位数字由NPS Lab协助提供。申请认证方在申请FCC 认证注册时，由 FCC CORES 所发出的一个10 位数值参考代号。对于第一次申请FCC ID的客户可在 FCC 网站免费申请。详细参阅：FCC FRN注册号链接：https://fjallfoss.fcc.gov/coresWeb/publicHome.do&lt;br /&gt;
&lt;br /&gt;
*需要提供Grantee Code（授权码）对于第一次申请 FCC ID的客户。可在申请 FRN号后。申请 Grantee Code(需付费约60美金)，只需申请一次。FCC Grantee Code授权码注册链接：https://fjallfoss.fcc.gov/oetcf/eas/forms/GranteeRegistration.cfm&lt;br /&gt;
&lt;br /&gt;
*FCC ID包括Grantee Code 公司代号(3位或5位字母或数值)，每个Grantee Code只代表一间公司。该3位或5位号码由FCC随机提供，并非由客户自定。一旦申请成功,即成为固定的号码，作为该公司所有申请FCC ID 号码的前3位或5位代号。以及Product code产品的代号(1-14位字母或数值)。所以产品 ID号，前三位或者五位为 Grantee Code，后面由申请商自编(最多 14位)，通常用产品型号做自编码。&lt;br /&gt;
&lt;br /&gt;
*The label location information 。 FCC label 位置及其规格（铭牌），必须标明大小尺寸，以及在产品上的位置。 FCC label须包含 FCC ID号和 FCC警语，如果 label尺寸小，可只标明 FCC ID号，但 FCC警语一定要写在使用手册中（用户说明书）。其它如生产商，产品名称型号等信息可自行决定是否写在 label中。&lt;br /&gt;
&lt;br /&gt;
*Operational Description (Theory of Operation, Functional Description)。简单的工作原理，功能描述，请对产品的功能，用途，信号流程，各功能电路相互关系，电源供电做一个简短的说明。&lt;br /&gt;
&lt;br /&gt;
*Block Diagrams原理方框图，必须标明电路中所用到的任何晶振频率。&lt;br /&gt;
&lt;br /&gt;
*Circuit Schematics电路图，请确保清晰，其位号也需要看得清。&lt;br /&gt;
&lt;br /&gt;
*简单的使用说明User Manual，用户手册或使用说明书。&lt;br /&gt;
&lt;br /&gt;
*授权信&lt;br /&gt;
&lt;br /&gt;
*保密信(如需要保密)&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;FCC ID认证样品准备&#039;&#039;&#039;==&lt;br /&gt;
*提供申请FCC ID需要的样机，至少2台，一台完整普通的类似出货样品，一台RF定频样机。&lt;br /&gt;
* 1~2套完整样品&lt;br /&gt;
* 1~2套定频样机&lt;br /&gt;
* 定频软件&lt;br /&gt;
* 定频方法&lt;br /&gt;
&lt;br /&gt;
 定频样机需要满足条件&lt;br /&gt;
&lt;br /&gt;
（1）连接有类似SMA接头的射频线&lt;br /&gt;
&lt;br /&gt;
（2）安装有定频软件或者提供定频软件&lt;br /&gt;
&lt;br /&gt;
（3）例如，蓝牙类产品一般需要提供定频板（控制板，链接电脑与样品的协议转换，即人机控制的桥梁）&lt;br /&gt;
&lt;br /&gt;
（4）满足测试需求（能定频或跳频，能持续发射等）&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;什么是定频？&#039;&#039;&#039;==&lt;br /&gt;
参阅 [[Fix_frequency|无线定频]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;FCC ID证书官方查询&#039;&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
网站：https://apps.fcc.gov/oetcf/eas/reports/GenericSearch.cfm&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=CE_RED&amp;diff=28</id>
		<title>CE RED</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=CE_RED&amp;diff=28"/>
		<updated>2019-08-26T06:23:58Z</updated>

		<summary type="html">&lt;p&gt;EMC：​/* 欧洲RED */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==&#039;&#039;&#039;欧洲CE RED&#039;&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
指的是RED(Radio Equipment Directive) 电子电器产品的无线电指令，所有去欧洲的相关有意发射的RF电子电器产品都需要满足相关电磁兼容的标准，例如欧洲的电信联盟ETSI标准。&lt;br /&gt;
&lt;br /&gt;
 Directive 2014/53/EU of the European Parliament and of the Council of 16 April 2014 on the harmonisation of the laws of the Member States relating to the making available on the market of radio equipment and repealing Directive 1999/5/EC Text with EEA relevance. Applicable as of 13 June 2016.&lt;br /&gt;
 OJ L 153, 22.5.2014&lt;br /&gt;
&lt;br /&gt;
 为适应欧盟新立法框架（New Legislative Framework，NLF），2014年5月22日，欧盟官方期刊(L 153/62)公布了新版本的无线电设备指令2014/53/EU，用以替换原有的无线电及电信终端设备指令1999/5/EC。从2017年6月13号起RED 2014/53/EU指令正式代替RTTE 1999/5/EC指令。 2018年6月12日起，无线电设备投放市场前，制造商应针对低水平符合基本要求的无线电设备在中心系统进行设备类型注册登记。&lt;br /&gt;
&lt;br /&gt;
 RED指令的目的是：确保更为简便的市场准入以及对消费者健康和安全，以及家禽和财产更高水平的保护。为防止有害干扰，无线电设备应具有足够的电磁兼容水平并能有效使用无线电频谱和支持无线电频谱的有效利用。RED指令覆盖安全Safety、电磁兼容性EMC及无线电频谱RF要求。RED所涵盖的无线电设备不受低电压指令（LVD）或电磁兼容性指令（EMC）的约束：这些指令的基本要求由RED的基本要求所覆盖，但有一定的修改。&lt;br /&gt;
&lt;br /&gt;
 RED指令覆盖范围：工作频率在3000 GHz以下的所有无线电设备。包括短距离通讯设备，宽频带设备和移动通讯设备等，还覆盖仅用于声音接收和电视广播服务的无线电设备（例如，FM收音机和电视机）。例如：27.145 MHz无线遥控玩具，433.92 MHz 无线遥控器，2.4 GHz 蓝牙音箱，2.4 GHz/5 GHz WIFI空调和手机等任何内部具有RF有意发射频率的电子电器。&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;CE RED认证需要提供的资料&#039;&#039;&#039;==&lt;br /&gt;
* 天线规格(或者天线增益图)&lt;br /&gt;
* 定频软件(也叫定频程式.使发射模块能够定在某一频率点持续发射,一般BT 和WIFI 一定要提供)&lt;br /&gt;
* Bill of Materials 元器件清单&lt;br /&gt;
* Block Diagram 原理框图&lt;br /&gt;
* Circuit Diagram 电路原理图&lt;br /&gt;
* Product Description and Concept of&lt;br /&gt;
* Operation 产品描述和工作原理描述&lt;br /&gt;
* Label Artwork标签丝印&lt;br /&gt;
* Marketing or Design 包装设计图&lt;br /&gt;
* PCB Layout 铜箔布线图&lt;br /&gt;
* Copy of Declaration of Conformity 符合性声明副本&lt;br /&gt;
* Sub‐Assemblies 装配图&lt;br /&gt;
* User Manual 用户手册&lt;br /&gt;
* Declaration on Model Difference 型号差异声明&lt;br /&gt;
* ISO 9001 Quality System Certification 质量体系证书&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;CE RED认证样品准备&#039;&#039;&#039;==&lt;br /&gt;
&lt;br /&gt;
* 1~2套完整样品&lt;br /&gt;
&lt;br /&gt;
* 1~2套定频样机&lt;br /&gt;
&lt;br /&gt;
* 定频软件&lt;br /&gt;
&lt;br /&gt;
* 定频方法&lt;br /&gt;
&lt;br /&gt;
 定频样机需要满足条件&lt;br /&gt;
&lt;br /&gt;
（1）连接有类似SMA接头的射频线&lt;br /&gt;
&lt;br /&gt;
（2）安装有定频软件或者提供定频软件&lt;br /&gt;
&lt;br /&gt;
（3）例如，蓝牙类产品一般需要提供定频板（控制板，链接电脑与样品的协议转换，即人机控制的桥梁）&lt;br /&gt;
&lt;br /&gt;
（4）满足测试需求（能定频或跳频，能持续发射等）&lt;br /&gt;
&lt;br /&gt;
==&#039;&#039;&#039;什么是定频？&#039;&#039;&#039;==&lt;br /&gt;
参阅 [[Fix_frequency|无线定频]]&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E5%8D%8E%E5%A4%AB%E7%83%A4%E9%A5%BC%E6%9C%BACE%E8%AE%A4%E8%AF%81&amp;diff=124</id>
		<title>华夫烤饼机CE认证</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E5%8D%8E%E5%A4%AB%E7%83%A4%E9%A5%BC%E6%9C%BACE%E8%AE%A4%E8%AF%81&amp;diff=124"/>
		<updated>2019-07-31T03:12:30Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;华夫烤饼机CE认证卖去欧洲需要满足什么标准呢？&lt;br /&gt;
&lt;br /&gt;
EMC&lt;br /&gt;
* IEC/EN 61000-3-2&lt;br /&gt;
* IEC/EN 61000-3-3&lt;br /&gt;
* CISPR 14-1 / EN 55014-1&lt;br /&gt;
* CISPR 14-2 / EN 55014-2&lt;br /&gt;
&lt;br /&gt;
Safety&lt;br /&gt;
* IEC / EN 60335-1&lt;br /&gt;
* IEC / EN 60335-2-9 &lt;br /&gt;
* IEC / EN 62233&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
如果是卖去海湾七国例如做做Gmark用IEC报告的话，那么IEC / EN 62233以及EMC标准就不用做了，满足IEC / EN 60335-1与IEC / EN 60335-2-9即可。&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=Blender%E6%90%85%E6%8B%8C%E6%9C%BA&amp;diff=20</id>
		<title>Blender搅拌机</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=Blender%E6%90%85%E6%8B%8C%E6%9C%BA&amp;diff=20"/>
		<updated>2019-07-31T03:07:14Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Blender搅拌机去欧洲，需要做哪些标准？&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EMC标准&#039;&#039;&#039;&lt;br /&gt;
 EN55014-1&lt;br /&gt;
 EN55014-2&lt;br /&gt;
 EN61000-3-2&lt;br /&gt;
 EN61000-3-3&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;LVD标准&#039;&#039;&#039;&lt;br /&gt;
 EN 60335-1&lt;br /&gt;
 EN 60335-2-14&lt;br /&gt;
 EN 62233:2008&lt;br /&gt;
&lt;br /&gt;
在安全通用标准IEC60335-1 中，对电动类器具的输入功率只有上偏差限制。在旧版标准IEC60335-2-14中，正常温升对电机的加载测试，只要不出现危险状况，允许电机绕组温升超过限值。&lt;br /&gt;
&lt;br /&gt;
但是，2016年发布的新版标准IEC60335-2-14:2016，对于正常温升时的测试功率要求更为严格。&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;新版要求如下：&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
* more than 80 % of rated power input for a rated power input not exceeding 300 W; &lt;br /&gt;
  额定功率≤300W，测试功率要超过额定功率的80%； &lt;br /&gt;
* more than rated power input minus 60 W for a rated power input between 300 W and 400 W; &lt;br /&gt;
  额定功率300W-400W，测试功率要超过（额定功率-60W）； &lt;br /&gt;
* more than 85 % of rated power input for a rated power input exceeding 400.  &lt;br /&gt;
  额定功率 &amp;gt;400W，测试功率要超过额定功率的85%。 &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;测试结果：电机绕组温升不能超过标准限值。&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
例如：搅拌机，额定功率800W，测试要求如下：&lt;br /&gt;
&lt;br /&gt;
此搅拌机的温升测试必须加载功率直到超过680W。&lt;br /&gt;
测试周期可以按说明书规定时间加1分钟（或按标准时间3分钟）；中间休息1分钟，共10个循环。&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=IVD&amp;diff=84</id>
		<title>IVD</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=IVD&amp;diff=84"/>
		<updated>2019-07-18T09:22:00Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; 欧盟为消除各成员国间的贸易壁垒，逐步建立成为一个统一的大市场，以确保人员、服务、资金和产品（如医疗器械）的自由流通。在医疗器械领域，欧盟委员会制定了三个欧盟指令，以替代原来各成员的认可体系，使有关这类产品投放市场的规定协调一致。&lt;br /&gt;
&lt;br /&gt;
这三个指令分别是：&lt;br /&gt;
* Medical devices Directive - MDD Directive 93/42/EEC&lt;br /&gt;
* In vitro diagnostic medical devices - IVD Directive 98/79/EC&lt;br /&gt;
* Active implantable medical devices - AIMD Directive 90/385/EEC 适用于心脏起搏器，可植入的胰岛素泵等有源植入性医疗器械。&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Directive 98/79/EC - IVD - In vitro diagnostic medical devices - 体外诊断医疗器械&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
体外诊断，即IVD(In Vitro Diagnosis)，是指在人体之外，通过对人体样本(血液、体液、组织等)进行检测而获取临床诊断信息，进而判断疾病或机体功能的产品和服务。体外诊断产品主要由诊断设备（仪器）和诊断试剂构成。根据我国国家药品监督管理局（NMPA）的《医疗器械分类目录》标准，体外诊断设备属于临床检验分析仪器类。&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;IVD体外诊断医疗器械产品分类&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
体外诊断仪器&lt;br /&gt;
* 按诊断方法分：临床化学分析仪器、免疫化学分析仪器、血液分析仪器、微生物分析仪器。&lt;br /&gt;
* 按搭配试剂分：开放式系统、封闭式系统。&lt;br /&gt;
&lt;br /&gt;
体外诊断试剂&lt;br /&gt;
* 按检验原理分：生化诊断试剂、免疫诊断试剂、分子诊断试剂、微生物诊断试剂、尿液诊断试剂、凝血类诊断试剂、血液学和流式细胞诊断试剂。&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;主要测试标准&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
* EN 61326-1 / GB 18268-1&lt;br /&gt;
* 测量，控制和实验室用电气设备。电磁兼容性要求。第1部分：一般要求&lt;br /&gt;
* Electrical equipment for measurement, control and laboratory use — EMC requirements — Part 1: General requirements&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
* EN 61326-2-6:2006 / GBT 18268.26-2010&lt;br /&gt;
* 测量，控制和实验室用电气设备 -  EMC要求 - 第2-6部分：特殊要求 - 体外诊断（IVD）医疗设备&lt;br /&gt;
* 测量控制和实验室用的电设备 电磁兼容性要求 第26部分：特殊要求 体外诊断 IVD 医疗设备&lt;br /&gt;
* Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;根据联盟协调立法公布的协调标准参考文献&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
* EN 556-1:2001/AC:2006 Sterilization of medical devices - Requirements for medical devices to be designated &amp;quot;STERILE&amp;quot; - Part 1: Requirements for terminally sterilized medical devices&lt;br /&gt;
&lt;br /&gt;
* EN 556-2:2015 Sterilization of medical devices - Requirements for medical devices to be designated &#039;&#039;STERILE&amp;quot; - Part 2: Requirements for aseptically processed medical devices&lt;br /&gt;
&lt;br /&gt;
* EN ISO 11137-1:2015 (new) Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006, including Amd 1:2013)&lt;br /&gt;
&lt;br /&gt;
* EN ISO 11137-2:2015 Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2013) Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (ISO 11737-2:2009)&lt;br /&gt;
&lt;br /&gt;
* EN 12322:1999 In vitro diagnostic medical devices - Culture media for microbiology - Performance criteria for culture media&lt;br /&gt;
&lt;br /&gt;
* EN ISO 13408-1:2015 Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008, including Amd 1:2013)&lt;br /&gt;
&lt;br /&gt;
* EN ISO 13408-2:2011 Aseptic processing of health care products - Part 2: Filtration (ISO 13408-2:2003)&lt;br /&gt;
&lt;br /&gt;
* EN ISO 13408-3:2011 Aseptic processing of health care products - Part 3: Lyophilization (ISO 13408-3:2006)&lt;br /&gt;
&lt;br /&gt;
* EN ISO 13408-4:2011 Aseptic processing of health care products - Part 4: Clean-in-place technologies (ISO 13408-4:2005)&lt;br /&gt;
&lt;br /&gt;
* EN ISO 13408-5:2011 Aseptic processing of health care products - Part 5: Sterilization in place (ISO 13408-5:2006)&lt;br /&gt;
&lt;br /&gt;
* EN ISO 13408-6:2011 Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2005)&lt;br /&gt;
&lt;br /&gt;
* EN ISO 13408-7:2015 Aseptic processing of health care products - Part 7: Alternative processes for medical devices and combination products (ISO 13408-7:2012)&lt;br /&gt;
&lt;br /&gt;
* EN ISO 13485:2016 (new) Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)&lt;br /&gt;
&lt;br /&gt;
* EN 13532:2002 General requirements for in vitro diagnostic medical devices for self-testing&lt;br /&gt;
&lt;br /&gt;
* EN 13612:2002 Performance evaluation of in vitro diagnostic medical devices&lt;br /&gt;
&lt;br /&gt;
* EN 13641:2002 Elimination or reduction of risk of infection related to in vitro diagnostic reagents&lt;br /&gt;
&lt;br /&gt;
* EN 13975:2003 Sampling procedures used for acceptance testing of in vitro diagnostic medical devices - Statistical aspects&lt;br /&gt;
&lt;br /&gt;
* EN 14136:2004 Use of external quality assessment schemes in the assessment of the performance of in vitro diagnostic examination procedures&lt;br /&gt;
&lt;br /&gt;
* EN 14254:2004 In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans&lt;br /&gt;
&lt;br /&gt;
* EN 14820:2004 Single-use containers for human venous blood specimen collection&lt;br /&gt;
&lt;br /&gt;
* EN ISO 14937:2009 Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices (ISO 14937:2009)&lt;br /&gt;
&lt;br /&gt;
* EN ISO 14971:2012 Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01)&lt;br /&gt;
&lt;br /&gt;
* EN ISO 15193:2009 In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for content and presentation of reference measurement procedures (ISO 15193:2009)&lt;br /&gt;
&lt;br /&gt;
* EN ISO 15194:2009 In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for certified reference materials and the content of supporting documentation (ISO 15194:2009)&lt;br /&gt;
&lt;br /&gt;
* EN ISO 15197:2015 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2013)&lt;br /&gt;
&lt;br /&gt;
* EN ISO 15223-1:2016 (new) Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements (ISO 15223-1:2016, Corrected version 2016-12-15)&lt;br /&gt;
&lt;br /&gt;
* EN ISO 17511:2003 In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values assigned to calibrators and control materials (ISO 17511:2003)&lt;br /&gt;
&lt;br /&gt;
* EN ISO 18113-1:2011 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)&lt;br /&gt;
&lt;br /&gt;
* EN ISO 18113-2:2011 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)&lt;br /&gt;
&lt;br /&gt;
* EN ISO 18113-3:2011 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009)&lt;br /&gt;
&lt;br /&gt;
* EN ISO 18113-4:2011 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009)&lt;br /&gt;
&lt;br /&gt;
* EN ISO 18113-5:2011 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009)&lt;br /&gt;
&lt;br /&gt;
* EN ISO 18153:2003 In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values for catalytic concentration of enzymes assigned to calibrators and control materials (ISO 18153:2003)&lt;br /&gt;
&lt;br /&gt;
* EN ISO 20776-1:2006 Clinical laboratory testing and in vitro diagnostic test systems - Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices - Part 1: Reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseases (ISO 20776-1:2006)&lt;br /&gt;
&lt;br /&gt;
* EN ISO 23640:2015 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)&lt;br /&gt;
&lt;br /&gt;
* EN 61010-2-101:2002 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment&lt;br /&gt;
&lt;br /&gt;
* IEC 61010-2-101:2002 (Modified)&lt;br /&gt;
&lt;br /&gt;
* EN 61326-2-6:2006  Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment&lt;br /&gt;
&lt;br /&gt;
* EN 62304:2006/AC:2008  Medical device software - Software life-cycle processes&lt;br /&gt;
&lt;br /&gt;
* EN 62366:2008Medical devices - Application of usability engineering to medical devices&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Refter to https://iec.emc.design/thread-4070-1-1.html&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=MDD&amp;diff=98</id>
		<title>MDD</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=MDD&amp;diff=98"/>
		<updated>2019-07-18T09:19:03Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; 欧盟为消除各成员国间的贸易壁垒，逐步建立成为一个统一的大市场，以确保人员、服务、资金和产品（如医疗器械）的自由流通。在医疗器械领域，欧盟委员会制定了三个欧盟指令，以替代原来各成员的认可体系，使有关这类产品投放市场的规定协调一致。&lt;br /&gt;
这三个指令分别是：&lt;br /&gt;
&lt;br /&gt;
* Medical devices Directive - MDD Directive 93/42/EEC&lt;br /&gt;
* In vitro diagnostic medical devices - IVD Directive 98/79/EC&lt;br /&gt;
* Active implantable medical devices - AIMD Directive 90/385/EEC  适用于心脏起搏器，可植入的胰岛素泵等有源植入性医疗器械。&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Directive 93/42/EEC 医疗器械MDD指令&#039;&#039;&#039;&lt;br /&gt;
* MDD医疗器械指令（MedicalDevicesDirective，93/42/EEC），适用范围很广，包括除有源植入性和体外诊断器械之外的几乎所有的医疗器械，如无源性医疗器械（敷料、一次性使用产品、接触镜、血袋、导管等）；以及有源性医疗器械，如核磁共振仪、超声诊断和治疗仪、输液泵等。该指令已于1995年1月1日生效，过渡截止日期为1998年6月13日从1998年6月14日起强制执行。&lt;br /&gt;
　　上述指令规定，在指令正式实施后，只有带有CE标志的医疗器械产品才能在欧盟市场上销售。&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Reference and title of the standard&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
* CEN	EN 285:2006+A2:2009Sterilization - Steam sterilizers - Large sterilizers	&lt;br /&gt;
* CEN	EN 455-1:2000Medical gloves for single use - Part 1: Requirements and testing for freedom from holes	&lt;br /&gt;
* CEN	EN 455-2:2009+A2:2013Medical gloves for single use - Part 2: Requirements and testing for physical properties	&lt;br /&gt;
* CEN	EN 455-3:2006Medical gloves for single use - Part 3: Requirements and testing for biological evaluation	&lt;br /&gt;
* CEN	EN 455-4:2009Medical gloves for single use - Part 4: Requirements and testing for shelf life determination	&lt;br /&gt;
* CEN	EN 556-1:2001Sterilization of medical devices - Requirements for medical devices to be designated &amp;quot;STERILE&amp;quot; - Part 1: Requirements for terminally sterilized medical devices	&lt;br /&gt;
* EN 556-1:2001/AC:2006&lt;br /&gt;
* CEN	EN 556-2:2015Sterilization of medical devices - Requirements for medical devices to be designated &#039;&#039;STERILE&amp;quot; - Part 2: Requirements for aseptically processed medical devices	&lt;br /&gt;
* CEN	EN 794-3:1998+A2:2009Lung ventilators - Part 3: Particular requirements for emergency and transport ventilators	&lt;br /&gt;
* CEN	EN 1041:2008Information supplied by the manufacturer of medical devices	&lt;br /&gt;
* CEN	EN 1060-3:1997+A2:2009Non-invasive sphygmomanometers - Part 3: Supplementary requirements for electro-mechanical blood pressure measuring systems	&lt;br /&gt;
* CEN	EN 1060-4:2004Non-invasive sphygmomanometers - Part 4: Test procedures to determine the overall system accuracy of automated non-invasive sphygmomanometers	&lt;br /&gt;
* CEN	EN ISO 1135-4:2011Transfusion equipment for medical use - Part 4: Transfusion sets for single use (ISO 1135-4:2010)	&lt;br /&gt;
* CEN	EN 1282-2:2005+A1:2009Tracheostomy tubes - Part 2: Paediatric tubes (ISO 5366-3:2001, modified)	&lt;br /&gt;
* CEN	EN 1422:1997+A1:2009Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods	&lt;br /&gt;
* CEN	EN 1618:1997Catheters other than intravascular catheters - Test methods for common properties	&lt;br /&gt;
* CEN	EN 1639:2009Dentistry - Medical devices for dentistry - Instruments	&lt;br /&gt;
* CEN	EN 1640:2009Dentistry - Medical devices for dentistry - Equipment			&lt;br /&gt;
* CEN	EN 1641:2009Dentistry - Medical devices for dentistry - Materials	&lt;br /&gt;
* CEN	EN 1642:2011Dentistry - Medical devices for dentistry - Dental implants	&lt;br /&gt;
* CEN	EN 1707:1996Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment - Lock fittings	&lt;br /&gt;
* CEN	EN 1782:1998+A1:2009Tracheal tubes and connectors	&lt;br /&gt;
* CEN	EN 1789:2007+A1:2010Medical vehicles and their equipment - Road ambulances	&lt;br /&gt;
* CEN	EN 1820:2005+A1:2009Anaesthetic reservoir bags (ISO 5362:2000, modified)	&lt;br /&gt;
* CEN	EN 1865-1:2010+A1:2015Patient handling equipment used in road ambulances - Part 1: General stretcher systems and patient handling equipment	&lt;br /&gt;
* CEN	EN 1865-2:2010+A1:2015Patient handling equipment used in road ambulances - Part 2: Power assisted stretcher	&lt;br /&gt;
* CEN	EN 1865-3:2012Patient handling equipment used in road ambulances - Part 3: Heavy duty stretcher	&lt;br /&gt;
* CEN	EN 1865-4:2012Patient handling equipment used in road ambulances - Part 4: Foldable patient transfer chair	&lt;br /&gt;
* CEN	EN 1865-5:2012Patient handling equipment used in road ambulances - Part 5: Stretcher support	&lt;br /&gt;
* CEN	EN 1985:1998Walking aids - General requirements and test methods	&lt;br /&gt;
* CEN	EN ISO 3826-2:2008Plastics collapsible containers for human blood and blood components - Part 2: Graphical symbols for use on labels and instruction leaflets (ISO 3826-2:2008)	&lt;br /&gt;
* CEN	EN ISO 3826-3:2007Plastics collapsible containers for human blood and blood components - Part 3: Blood bag systems with integrated features (ISO 3826-3:2006)	&lt;br /&gt;
* CEN	EN ISO 3826-4:2015Plastics collapsible containers for human blood and blood components - Part 4: Aphaeresis blood bag systems with integrated features (ISO 3826-4:2015)	&lt;br /&gt;
* CEN	EN ISO 4074:2002Natural latex rubber condoms - Requirements and test methods (ISO 4074:2002)	&lt;br /&gt;
* CEN	EN ISO 4135:2001Anaesthetic and respiratory equipment - Vocabulary (ISO 4135:2001)	&lt;br /&gt;
* CEN	EN ISO 5359:2008Low-pressure hose assemblies for use with medical gases (ISO 5359:2008)	&lt;br /&gt;
* EN ISO    5359:2008/A1:2011&lt;br /&gt;
* CEN	EN ISO 5360:2009Anaesthetic vaporizers - Agent-specific filling systems (ISO 5360:2006)	&lt;br /&gt;
* CEN	EN ISO 5366-1:2009Anaesthetic and respiratory equipment - Tracheostomy tubes - Part 1: Tubes and connectors for use in adults (ISO 5366-1:2000)	&lt;br /&gt;
* CEN	EN ISO 5840:2009Cardiovascular implants - Cardiac valve prostheses (ISO 5840:2005)	&lt;br /&gt;
* CEN	EN ISO 7197:2009Neurosurgical implants - Sterile, single-use hydrocephalus shunts and components (ISO 7197:2006, including Cor 1:2007)	&lt;br /&gt;
* CEN	EN ISO 7376:2009Anaesthetic and respiratory equipment - Laryngoscopes for tracheal intubation (ISO 7376:2009)	&lt;br /&gt;
* CEN	EN ISO 7396-1:2007Medical gas pipeline systems - Part 1: Pipeline systems for compressed medical gases and vacuum (ISO 7396-1:2007)	&lt;br /&gt;
* EN ISO   7396-1:2007/A1:2010&lt;br /&gt;
* EN ISO   7396-1:2007/A2:2010&lt;br /&gt;
* CEN	EN ISO 7396-2:2007Medical gas pipeline systems - Part 2: Anaesthetic gas scavenging disposal systems (ISO 7396-2:2007)	&lt;br /&gt;
* CEN	EN ISO 7886-3:2009Sterile hypodermic syringes for single use - Part 3: Auto-disable syringes for fixed-dose immunization (ISO 7886-3:2005)	&lt;br /&gt;
* CEN	EN ISO 7886-4:2009Sterile hypodermic syringes for single use - Part 4: Syringes with re-use prevention feature (ISO 7886-4:2006)	&lt;br /&gt;
* CEN	EN ISO 8185:2009Respiratory tract humidifiers for medical use - Particular requirements for respiratory humidification systems (ISO 8185:2007)	&lt;br /&gt;
* CEN	EN ISO 8359:2009Oxygen concentrators for medical use - Safety requirements (ISO 8359:1996)	&lt;br /&gt;
* EN ISO   8359:2009/A1:2012&lt;br /&gt;
* CEN	EN ISO 8835-2:2009Inhalational anaesthesia systems - Part 2: Anaesthetic breathing systems (ISO 8835-2:2007)	&lt;br /&gt;
* CEN	EN ISO 8835-3:2009Inhalational anaesthesia systems - Part 3: Transfer and receiving systems of active anaesthetic gas scavenging systems (ISO 8835-3:2007)	&lt;br /&gt;
* EN ISO    8835-3:2009/A1:2010&lt;br /&gt;
* CEN	EN ISO 8835-4:2009Inhalational anaesthesia systems - Part 4: Anaesthetic vapour delivery devices (ISO 8835-4:2004)	&lt;br /&gt;
* CEN	EN ISO 8835-5:2009Inhalational anaesthesia systems - Part 5: Anaesthetic ventilators (ISO 8835-5:2004)	&lt;br /&gt;
* CEN	EN ISO 9170-1:2008Terminal units for medical gas pipeline systems - Part 1: Terminal units for use with compressed medical gases and vacuum (ISO 9170-1:2008)	&lt;br /&gt;
* CEN	EN ISO 9170-2:2008Terminal units for medical gas pipeline systems - Part 2: Terminal units for anaesthetic gas scavenging systems (ISO 9170-2:2008)	&lt;br /&gt;
* CEN	EN ISO 9360-1:2009Anaesthetic and respiratory equipment - Heat and moisture exchangers (HMEs) for humidifying respired gases in humans - Part 1: HMEs for use with minimum tidal volumes of 250 ml (ISO 9360-1:2000)	&lt;br /&gt;
* CEN	EN ISO 9360-2:2009Anaesthetic and respiratory equipment - Heat and moisture exchangers (HMEs) for humidifying respired gases in humans - Part 2: HMEs for use with tracheostomized patients having minimum tidal volumes of 250 ml (ISO 9360-2:2001)	&lt;br /&gt;
* CEN	EN ISO 9713:2009Neurosurgical implants - Self-closing intracranial aneurysm clips (ISO 9713:2002)	&lt;br /&gt;
* CEN	EN ISO 10079-1:2009Medical suction equipment - Part 1: Electrically powered suction equipment - Safety requirements (ISO 10079-1:1999)	&lt;br /&gt;
* CEN	EN ISO 10079-2:2009Medical suction equipment - Part 2: Manually powered suction equipment (ISO 10079-2:1999)	&lt;br /&gt;
* CEN	EN ISO 10079-3:2009Medical suction equipment - Part 3: Suction equipment powered from a vacuum or pressure source (ISO 10079-3:1999)	&lt;br /&gt;
* CEN	EN ISO 10328:2016 (new)Prosthetics - Structural testing of lower-limb prostheses - Requirements and test methods (ISO 10328:2016)	&lt;br /&gt;
* CEN	EN ISO 10524-1:2006Pressure regulators for use with medical gases - Part 1: Pressure regulators and pressure regulators with flow-metering devices (ISO 10524-1:2006)	&lt;br /&gt;
* CEN	EN ISO 10524-2:2006Pressure regulators for use with medical gases - Part 2: Manifold and line pressure regulators (ISO 10524-2:2005)	&lt;br /&gt;
* CEN	EN ISO 10524-3:2006Pressure regulators for use with medical gases - Part 3: Pressure regulators integrated with cylinder valves (ISO 10524-3:2005)	&lt;br /&gt;
* CEN	EN ISO 10524-4:2008Pressure regulators for use with medical gases - Part 4: Low-pressure regulators (ISO 10524-4:2008)	&lt;br /&gt;
* CEN	EN ISO 10535:2006Hoists for the transfer of disabled persons - Requirements and test methods (ISO 10535:2006)	&lt;br /&gt;
* CEN	EN ISO 10555-1:2009Sterile, single-use intravascular catheters - Part 1: General requirements (ISO 10555-1:1995, including Amd 1:1999 and Amd 2:2004)	&lt;br /&gt;
* CEN	EN ISO 10651-2:2009Lung ventilators for medical use - Particular requirements for basic safety and essential performance - Part 2: Home care ventilators for ventilator-dependent patients (ISO 10651-2:2004)	&lt;br /&gt;
* CEN	EN ISO 10651-4:2009Lung ventilators - Part 4: Particular requirements for operator-powered resuscitators (ISO 10651-4:2002)	&lt;br /&gt;
* CEN	EN ISO 10651-6:2009Lung ventilators for medical use - Particular requirements for basic safety and essential performance - Part 6: Home-care ventilatory support devices (ISO 10651-6:2004)	&lt;br /&gt;
* CEN	EN ISO 10993-1:2009Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2009)	&lt;br /&gt;
* EN ISO 10993-1:2009/AC:2010&lt;br /&gt;
* CEN	EN ISO 10993-3:2014Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2014)	&lt;br /&gt;
* CEN	EN ISO 10993-4:2009Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002, including Amd 1:2006)	&lt;br /&gt;
* CEN	EN ISO 10993-5:2009Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)	&lt;br /&gt;
* CEN	EN ISO 10993-6:2009Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007)	&lt;br /&gt;
* CEN	EN ISO 10993-7:2008Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008)	&lt;br /&gt;
* EN ISO 10993-7:2008/AC:2009&lt;br /&gt;
* CEN	EN ISO 10993-9:2009Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:2009)	&lt;br /&gt;
* CEN	EN ISO 10993-11:2009Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006)	&lt;br /&gt;
* CEN	EN ISO 10993-12:2012Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012)	&lt;br /&gt;
* CEN	EN ISO 10993-13:2010Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010)	&lt;br /&gt;
* CEN	EN ISO 10993-14:2009Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)	&lt;br /&gt;
* CEN	EN ISO 10993-15:2009Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000)	&lt;br /&gt;
* CEN	EN ISO 10993-16:2010Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2010)	&lt;br /&gt;
* CEN	EN ISO 10993-17:2009Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)	&lt;br /&gt;
* CEN	EN ISO 10993-18:2009Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005)	&lt;br /&gt;
* CEN	EN ISO 11135-1:2007Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11135-1:2007)	&lt;br /&gt;
* CEN	EN ISO 11137-1:2015Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006, including Amd 1:2013)	&lt;br /&gt;
* CEN	EN ISO 11137-2:2015Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2013)	&lt;br /&gt;
* CEN	EN ISO 11138-2:2009Sterilization of health care products - Biological indicators - Part 2: Biological indicators for ethylene oxide sterilization processes (ISO 11138-2:2006)	&lt;br /&gt;
* CEN	EN ISO 11138-3:2009Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes (ISO 11138-3:2006)	&lt;br /&gt;
* CEN	EN ISO 11140-1:2009Sterilization of health care products - Chemical indicators - Part 1: General requirements (ISO 11140-1:2005)	&lt;br /&gt;
* CEN	EN ISO 11140-3:2009Sterilization of health care products - Chemical indicators - Part 3: Class 2 indicator systems for use in the Bowie and Dick-type steam penetration test (ISO 11140-3:2007, including Cor 1:2007)	&lt;br /&gt;
* CEN	EN ISO 11197:2009Medical supply units (ISO 11197:2004)	&lt;br /&gt;
* CEN	EN ISO 11607-1:2009Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2006)	&lt;br /&gt;
* CEN	EN ISO 11607-2:2006Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006)	&lt;br /&gt;
* CEN	EN ISO 11737-1:2006Sterilization of medical devices - Microbiological methods - Part 1: Determination of a population of microorganisms on products (ISO 11737-1:2006)	&lt;br /&gt;
* EN ISO 11737-1:2006/AC:2009&lt;br /&gt;
* CEN	EN ISO 11737-2:2009Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (ISO 11737-2:2009)	&lt;br /&gt;
* CEN	EN ISO 11810-1:2009Lasers and laser-related equipment - Test method and classification for the laser resistance of surgical drapes and/or patient protective covers - Part 1: Primary ignition and penetration (ISO 11810-1:2005)	&lt;br /&gt;
* CEN	EN ISO 11810-2:2009Lasers and laser-related equipment - Test method and classification for the laser-resistance of surgical drapes and/or patient-protective covers - Part 2: Secondary ignition (ISO 11810-2:2007)	&lt;br /&gt;
* CEN	EN ISO 11979-8:2009Ophthalmic implants - Intraocular lenses - Part 8: Fundamental requirements (ISO 11979-8:2006)	&lt;br /&gt;
* CEN	EN ISO 11990-1:2014Lasers and laser-related equipment - Determination of laser resistance of tracheal tubes - Part 1: Tracheal tube shaft (ISO 11990-1:2011)	&lt;br /&gt;
* CEN	EN ISO 11990-2:2014Lasers and laser-related equipment - Determination of laser resistance of tracheal tubes - Part 2: Tracheal tube cuffs (ISO 11990-2:2010)	&lt;br /&gt;
* CEN	EN 12006-2:1998+A1:2009Non active surgical implants - Particular requirements for cardiac and vascular implants - Part 2: Vascular prostheses including cardiac valve conduits	&lt;br /&gt;
* CEN	EN 12006-3:1998+A1:2009Non active surgical implants - Particular requirements for cardiac and vascular implants - Part 3: Endovascular devices	&lt;br /&gt;
* CEN	EN 12183:2009Manual wheelchairs - Requirements and test methods	&lt;br /&gt;
* CEN	EN 12184:2009Electrically powered wheelchairs, scooters and their chargers - Requirements and test methods	&lt;br /&gt;
* CEN	EN 12342:1998+A1:2009Breathing tubes intended for use with anaesthetic apparatus and ventilators	&lt;br /&gt;
* CEN	EN 12470-1:2000+A1:2009Clinical thermometers - Part 1: Metallic liquid-in-glass thermometers with maximum device	&lt;br /&gt;
* CEN	EN 12470-2:2000+A1:2009Clinical thermometers - Part 2: Phase change type (dot matrix) thermometers	&lt;br /&gt;
* CEN	EN 12470-3:2000+A1:2009Clinical thermometers - Part 3: Performance of compact electrical thermometers (non-predictive and predictive) with maximum device	&lt;br /&gt;
* CEN	EN 12470-4:2000+A1:2009Clinical thermometers - Part 4: Performance of electrical thermometers for continuous measurement	&lt;br /&gt;
* CEN	EN 12470-5:2003Clinical thermometers - Part 5: Performance of infra-red ear thermometers (with maximum device)	&lt;br /&gt;
* CEN	EN ISO 12870:2009Ophthalmic optics - Spectacle frames - Requirements and test methods (ISO 12870:2004)	&lt;br /&gt;
* CEN	EN 13060:2014Small steam sterilizers	&lt;br /&gt;
* CEN	EN ISO 13408-1:2015Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008, including Amd 1:2013)	&lt;br /&gt;
* CEN	EN ISO 13408-2:2011Aseptic processing of health care products - Part 2: Filtration (ISO 13408-2:2003)	&lt;br /&gt;
* CEN	EN ISO 13408-3:2011Aseptic processing of health care products - Part 3: Lyophilization (ISO 13408-3:2006)	&lt;br /&gt;
* CEN	EN ISO 13408-4:2011Aseptic processing of health care products - Part 4: Clean-in-place technologies (ISO 13408-4:2005)	&lt;br /&gt;
* CEN	EN ISO 13408-5:2011Aseptic processing of health care products - Part 5: Sterilization in place (ISO 13408-5:2006)	&lt;br /&gt;
* CEN	EN ISO 13408-6:2011Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2005)	&lt;br /&gt;
* CEN	EN ISO 13408-7:2015Aseptic processing of health care products - Part 7: Alternative processes for medical devices and combination products (ISO 13408-7:2012)	&lt;br /&gt;
* CEN	EN ISO 13485:2016 (new)Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)	&lt;br /&gt;
* EN ISO 13485:2016/AC:2016 (new)&lt;br /&gt;
* CEN	EN 13544-1:2007+A1:2009Respiratory therapy equipment - Part 1: Nebulizing systems and their components	&lt;br /&gt;
* CEN	EN 13544-2:2002+A1:2009Respiratory therapy equipment - Part 2: Tubing and connectors	&lt;br /&gt;
* CEN	EN 13544-3:2001+A1:2009Respiratory therapy equipment - Part 3: Air entrainment devices	&lt;br /&gt;
* CEN	EN 13624:2003Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal activity of chemical disinfectants for instruments used in the medical area - Test method and requirements (phase 2, step 1)	&lt;br /&gt;
* CEN	EN 13718-1:2008Medical vehicles and their equipment - Air ambulances - Part 1: Requirements for medical devices used in air ambulances	&lt;br /&gt;
* CEN	EN 13718-2:2015Medical vehicles and their equipment - Air ambulances - Part 2: Operational and technical requirements for air ambulances	&lt;br /&gt;
* CEN	EN 13726-1:2002Test methods for primary wound dressings - Part 1: Aspects of absorbency	&lt;br /&gt;
* EN 13726-1:2002/AC:2003&lt;br /&gt;
* CEN	EN 13726-2:2002Test methods for primary wound dressings - Part 2: Moisture vapour transmission rate of permeable film dressings	&lt;br /&gt;
* CEN	EN 13727:2012Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity in the medical area - Test method and requirements (phase 2, step 1)	&lt;br /&gt;
* CEN	EN 13867:2002+A1:2009Concentrates for haemodialysis and related therapies	&lt;br /&gt;
* CEN	EN 13976-1:2011Rescue systems - Transportation of incubators - Part 1: Interface conditions	&lt;br /&gt;
* CEN	EN 13976-2:2011Rescue systems - Transportation of incubators - Part 2: System requirements	&lt;br /&gt;
* CEN	EN 14079:2003Non-active medical devices - Performance requirements and test methods for absorbent cotton gauze and absorbent cotton and viscose gauze	&lt;br /&gt;
* CEN	EN 14139:2010Ophthalmic optics - Specifications for ready-to-wear spectacles	&lt;br /&gt;
* CEN	EN ISO 14155:2011Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)	&lt;br /&gt;
* EN ISO 14155:2011/AC:2011 (new)&lt;br /&gt;
* CEN	EN 14180:2003+A2:2009Sterilizers for medical purposes - Low temperature steam and formaldehyde sterilizers - Requirements and testing	&lt;br /&gt;
* CEN	EN 14348:2005Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of mycobactericidal activity of chemical disinfectants in the medical area including instrument disinfectants - Test methods and requirements (phase 2, step 1)	&lt;br /&gt;
* CEN	EN ISO 14408:2009Tracheal tubes designed for laser surgery - Requirements for marking and accompanying information (ISO 14408:2005)	&lt;br /&gt;
* CEN	EN 14561:2006Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of bactericidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2)	&lt;br /&gt;
* CEN	EN 14562:2006Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of fungicidal or yeasticidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2)	&lt;br /&gt;
* CEN	EN 14563:2008Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of mycobactericidal or tuberculocidal activity of chemical disinfectants used for instruments in the medical area - Test method and requirements (phase 2, step 2)	&lt;br /&gt;
* CEN	EN ISO 14602:2011Non-active surgical implants - Implants for osteosynthesis - Particular requirements (ISO 14602:2010)	&lt;br /&gt;
* CEN	EN ISO 14607:2009Non-active surgical implants - Mammary implants - Particular requirements (ISO 14607:2007)	&lt;br /&gt;
* CEN	EN ISO 14630:2009Non-active surgical implants - General requirements (ISO 14630:2008)	&lt;br /&gt;
* CEN	EN 14683:2005Surgical masks - Requirements and test methods	&lt;br /&gt;
* CEN	EN ISO 14889:2009Ophthalmic optics - Spectacle lenses - Fundamental requirements for uncut finished lenses (ISO 14889:2003)	&lt;br /&gt;
* CEN	EN 14931:2006Pressure vessels for human occupancy (PVHO) - Multi-place pressure chamber systems for hyperbaric therapy - Performance, safety requirements and testing	&lt;br /&gt;
* CEN	EN ISO 14937:2009Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices (ISO 14937:2009)	&lt;br /&gt;
* CEN	EN ISO 14971:2012Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01)	&lt;br /&gt;
* CEN	EN ISO 15001:2011Anaesthetic and respiratory equipment - Compatibility with oxygen (ISO 15001:2010)	&lt;br /&gt;
* CEN	EN ISO 15002:2008Flow-metering devices for connection to terminal units of medical gas pipeline systems (ISO 15002:2008)	&lt;br /&gt;
* CEN	EN ISO 15004-1:2009Ophthalmic instruments - Fundamental requirements and test methods - Part 1: General requirements applicable to all ophthalmic instruments (ISO 15004-1:2006)	&lt;br /&gt;
* CEN	EN ISO 15223-1:2016 (new)Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements (ISO 15223-1:2016, Corrected version 2017-03)	&lt;br /&gt;
* CEN	EN ISO 15747:2011Plastic containers for intravenous injections (ISO 15747:2010)	&lt;br /&gt;
* CEN	EN ISO 15798:2010Ophthalmic implants - Ophthalmic viscosurgical devices (ISO 15798:2010)	&lt;br /&gt;
* CEN	EN ISO 15883-1:2009Washer-disinfectors - Part 1: General requirements, terms and definitions and tests (ISO 15883-1:2006)	&lt;br /&gt;
* CEN	EN ISO 15883-2:2009Washer-disinfectors - Part 2: Requirements and tests for washer-disinfectors employing thermal disinfection for surgical instruments, anaesthetic equipment, bowls, dishes, receivers, utensils, glassware, etc. (ISO 15883-2:2006)	&lt;br /&gt;
* CEN	EN ISO 15883-3:2009Washer-disinfectors - Part 3: Requirements and tests for washer-disinfectors employing thermal disinfection for human waste containers (ISO 15883-3:2006)	&lt;br /&gt;
* CEN	EN ISO 15883-4:2009Washer-disinfectors - Part 4: Requirements and tests for washer-disinfectors employing chemical disinfection for thermolabile endoscopes (ISO 15883-4:2008)	&lt;br /&gt;
* CEN	EN 15986:2011Symbol for use in the labelling of medical devices - Requirements for labelling of medical devices containing phthalates	&lt;br /&gt;
* CEN	EN ISO 16061:2009Instrumentation for use in association with non-active surgical implants - General requirements (ISO 16061:2008, Corrected version 2009-03-15)	&lt;br /&gt;
* CEN	EN ISO 16201:2006Technical aids for disabled persons - Environmental control systems for daily living (ISO 16201:2006)	&lt;br /&gt;
* CEN	EN ISO 17510-1:2009Sleep apnoea breathing therapy - Part 1: Sleep apnoea breathing therapy equipment (ISO 17510-1:2007)	&lt;br /&gt;
* CEN	EN ISO 17510-2:2009Sleep apnoea breathing therapy - Part 2: Masks and application accessories (ISO 17510-2:2007)	&lt;br /&gt;
* CEN	EN ISO 17664:2004Sterilization of medical devices - Information to be provided by the manufacturer for the processing of resterilizable medical devices (ISO 17664:2004)	&lt;br /&gt;
* CEN	EN ISO 17665-1:2006Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665-1:2006)	&lt;br /&gt;
* CEN	EN ISO 18777:2009Transportable liquid oxygen systems for medical use - Particular requirements (ISO 18777:2005)	&lt;br /&gt;
* CEN	EN ISO 18778:2009Respiratory equipment - Infant monitors - Particular requirements (ISO 18778:2005)	&lt;br /&gt;
* CEN	EN ISO 18779:2005Medical devices for conserving oxygen and oxygen mixtures - Particular requirements (ISO 18779:2005)	&lt;br /&gt;
* CEN	EN ISO 19054:2006Rail systems for supporting medical equipment (ISO 19054:2005)	&lt;br /&gt;
* CEN	EN 20594-1:1993Conical fittings with a 6% (Luer) taper for syringes, needles and certain other medical equipment - Part 1: General requirements (ISO 594-1:1986)	&lt;br /&gt;
* EN 20594-1:1993/A1:1997&lt;br /&gt;
* EN 20594-1:1993/AC:1996&lt;br /&gt;
* CEN	EN ISO 21534:2009Non-active surgical implants - Joint replacement implants - Particular requirements (ISO 21534:2007)	&lt;br /&gt;
* CEN	EN ISO 21535:2009Non-active surgical implants - Joint replacement implants - Specific requirements for hip-joint replacement implants (ISO 21535:2007)	&lt;br /&gt;
* CEN	EN ISO 21536:2009Non-active surgical implants - Joint replacement implants - Specific requirements for knee-joint replacement implants (ISO 21536:2007)	&lt;br /&gt;
* CEN	EN ISO 21649:2009Needle-free injectors for medical use - Requirements and test methods (ISO 21649:2006)	&lt;br /&gt;
* CEN	EN ISO 21969:2009High-pressure flexible connections for use with medical gas systems (ISO 21969:2009)	&lt;br /&gt;
* CEN	EN ISO 21987:2009Ophthalmic optics - Mounted spectacle lenses (ISO 21987:2009)	&lt;br /&gt;
* CEN	EN ISO 22442-1:2007Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management (ISO 22442-1:2007)	&lt;br /&gt;
* CEN	EN ISO 22442-2:2007Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO 22442-2:2007)	&lt;br /&gt;
* CEN	EN ISO 22442-3:2007Medical devices utilizing animal tissues and their derivatives - Part 3: Validation of the elimination and/or inactivation of viruses and transmissible spongiform encephalopathy (TSE) agents (ISO 22442-3:2007)	&lt;br /&gt;
* CEN	EN ISO 22523:2006External limb prostheses and external orthoses - Requirements and test methods (ISO 22523:2006)	&lt;br /&gt;
* CEN	EN ISO 22675:2016 (new)Prosthetics - Testing of ankle-foot devices and foot units - Requirements and test methods (ISO 22675:2016)	&lt;br /&gt;
* CEN	EN ISO 23328-1:2008Breathing system filters for anaesthetic and respiratory use - Part 1: Salt test method to assess filtration performance (ISO 23328-1:2003)	&lt;br /&gt;
* CEN	EN ISO 23328-2:2009Breathing system filters for anaesthetic and respiratory use - Part 2: Non-filtration aspects (ISO 23328-2:2002)	&lt;br /&gt;
* CEN	EN ISO 23747:2009Anaesthetic and respiratory equipment - Peak expiratory flow meters for the assessment of pulmonary function in spontaneously breathing humans (ISO 23747:2007)	&lt;br /&gt;
* CEN	EN ISO 25539-1:2009Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses (ISO 25539-1:2003 including Amd 1:2005)	&lt;br /&gt;
* EN ISO   25539-1:2009/AC:2011&lt;br /&gt;
* CEN	EN ISO 25539-2:2009Cardiovascular implants - Endovascular devices - Part 2: Vascular stents (ISO 25539-2:2008)	&lt;br /&gt;
* EN ISO   25539-2:2009/AC:2011&lt;br /&gt;
* CEN	EN ISO 26782:2009Anaesthetic and respiratory equipment - Spirometers intended for the measurement of time forced expired volumes in humans (ISO 26782:2009)	&lt;br /&gt;
* EN ISO   26782:2009/AC:2009&lt;br /&gt;
* CEN	EN 27740:1992Instruments for surgery, scalpels with detachable blades, fitting dimensions (ISO 7740:1985)	&lt;br /&gt;
* EN 27740:1992/A1:1997&lt;br /&gt;
* EN 27740:1992/AC:1996&lt;br /&gt;
* EN ISO 81060-1:2012Non-invasive sphygmomanometers - Part 1: Requirements and test methods for non-automated measurement type (ISO 81060-1:2007)	&lt;br /&gt;
* EN 60118-13:2005Electroacoustics - Hearing aids -- Part 13: Electromagnetic compatibility (EMC)&lt;br /&gt;
* IEC 60118-13:2004	&lt;br /&gt;
* EN 60522:1999Determination of the permanent filtration of X-ray tube assemblies&lt;br /&gt;
* IEC 60522:1999	&lt;br /&gt;
* EN 60580:2000Medical electrical equipment - Dose area product meters&lt;br /&gt;
* IEC 60580:2000	&lt;br /&gt;
* EN 60601-1:2006Medical electrical equipment - Part 1: General requirements for basic safety and essential performance&lt;br /&gt;
* IEC 60601-1:2005	&lt;br /&gt;
* EN 60601-1:2006/AC:2010&lt;br /&gt;
* EN 60601-1:2006/A1:2013&lt;br /&gt;
* IEC 60601-1:2005/A1:2012&lt;br /&gt;
* EN 60601-1-1:2001Medical electrical equipment - Part 1-1: General requirements for safety - Collateral standard: Safety requirements for medical electrical systems&lt;br /&gt;
* IEC 60601-1-1:2000	&lt;br /&gt;
* EN 60601-1-2:2015Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests&lt;br /&gt;
* IEC 60601-1-2:2014	&lt;br /&gt;
* EN 60601-1-3:2008Medical electrical equipment - Part 1-3: General requirements for basic safety and essential performance - Collateral Standard: Radiation protection in diagnostic X-ray equipment&lt;br /&gt;
* IEC 60601-1-3:2008	&lt;br /&gt;
* EN 60601-1-3:2008/AC:2010&lt;br /&gt;
* EN 60601-1-3:2008/A11:2016 (new)&lt;br /&gt;
* EN 60601-1-4:1996Medical electrical equipment - Part 1-4: General requirements for safety - Collateral standard: Programmable electrical medical systems&lt;br /&gt;
* IEC 60601-1-4:1996	&lt;br /&gt;
* EN 60601-1-4:1996/A1:1999&lt;br /&gt;
* IEC 60601-1-4:1996/A1:1999&lt;br /&gt;
* EN 60601-1-6:2010Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability&lt;br /&gt;
* IEC 60601-1-6:2010	&lt;br /&gt;
* EN 60601-1-8:2007Medical electrical equipment - Part 1-8: General requirements for basic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems&lt;br /&gt;
* IEC 60601-1-8:2006	&lt;br /&gt;
* EN 60601-1-8:2007/AC:2010&lt;br /&gt;
* EN 60601-1-8:2007/A11:2017 (new)&lt;br /&gt;
* EN 60601-1-10:2008Medical electrical equipment - Part 1-10: General requirements for basic safety and essential performance - Collateral Standard: Requirements for the development of physiologic closed-loop controllers&lt;br /&gt;
* IEC 60601-1-10:2007	&lt;br /&gt;
* EN 60601-1-11:2010Medical electrical equipment - Part 1-11: General requirements for basic safety and essential performance - Collateral standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment&lt;br /&gt;
* IEC 60601-1-11:2010	&lt;br /&gt;
* EN 60601-2-1:1998Medical electrical equipment - Part 2-1: Particular requirements for the safety of electron accelerators in the range of 1 MeV to 50 MeV&lt;br /&gt;
* IEC 60601-2-1:1998	&lt;br /&gt;
* EN 60601-2-1:1998/A1:2002&lt;br /&gt;
* IEC 60601-2-1:1998/A1:2002&lt;br /&gt;
* EN 60601-2-2:2009Medical electrical equipment - Part 2-2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories&lt;br /&gt;
* IEC 60601-2-2:2009	&lt;br /&gt;
* EN 60601-2-3:1993Medical electrical equipment - Part 2: Particular requirements for the safety of short-wave therapy equipment&lt;br /&gt;
* IEC 60601-2-3:1991	&lt;br /&gt;
* EN 60601-2-3:1993/A1:1998&lt;br /&gt;
* IEC 60601-2-3:1991/A1:1998&lt;br /&gt;
* EN 60601-2-4:2003Medical electrical equipment -- Part 2-4: Particular requirements for the safety of cardiac defibrillators&lt;br /&gt;
* IEC 60601-2-4:2002	&lt;br /&gt;
* EN 60601-2-5:2000Medical electrical equipment - Part 2-5: Particular requirements for the safety of ultrasonic physiotherapy equipment&lt;br /&gt;
* IEC 60601-2-5:2000	&lt;br /&gt;
* EN 60601-2-8:1997Medical electrical equipment - Part 2: Particular requirements for the safety of therapeutic X-ray equipment operating in the range 10 kV to 1 MV&lt;br /&gt;
* IEC 60601-2-8:1987	&lt;br /&gt;
* EN 60601-2-8:1997/A1:1997&lt;br /&gt;
* IEC 60601-2-8:1987/A1:1997&lt;br /&gt;
* EN 60601-2-10:2000Medical electrical equipment - Part 2-10: Particular requirements for the safety of nerve and muscle stimulators&lt;br /&gt;
* IEC 60601-2-10:1987	&lt;br /&gt;
* EN 60601-2-10:2000/A1:2001&lt;br /&gt;
* IEC 60601-2-10:1987/A1:2001&lt;br /&gt;
* EN 60601-2-11:1997Medical electrical equipment - Part 2-11: Particular requirements for the safety of gamma beam therapy equipment&lt;br /&gt;
* IEC 60601-2-11:1997	&lt;br /&gt;
* EN 60601-2-11:1997/A1:2004&lt;br /&gt;
* IEC 60601-2-11:1997/A1:2004&lt;br /&gt;
* EN 60601-2-12:2006Medical electrical equipment - Part 2-12: Particular requirements for the safety of lung ventilators - Critical care ventilators&lt;br /&gt;
* IEC 60601-2-12:2001	&lt;br /&gt;
* EN 60601-2-13:2006Medical electrical equipment - Part 2-13: Particular requirements for the safety and essential performance of anaesthetic systems&lt;br /&gt;
* IEC 60601-2-13:2003	&lt;br /&gt;
* EN 60601-2-13:2006/A1:2007&lt;br /&gt;
* IEC 60601-2-13:2003/A1:2006&lt;br /&gt;
* EN 60601-2-16:1998Medical electrical equipment - Part 2-16: Particular requirements for the safety of haemodialysis, haemodiafiltration and haemofiltration equipment&lt;br /&gt;
* IEC 60601-2-16:1998	&lt;br /&gt;
* EN 60601-2-16:1998/AC:1999&lt;br /&gt;
* EN 60601-2-17:2004Medical electrical equipment - Part 2-17: Particular requirements for the safety of automatically-controlled brachytherapy afterloading equipment&lt;br /&gt;
* IEC 60601-2-17:2004	&lt;br /&gt;
* EN 60601-2-18:1996Medical electrical equipment - Part 2: Particular requirements for the safety of endoscopic equipment&lt;br /&gt;
* IEC 60601-2-18:1996	&lt;br /&gt;
* EN 60601-2-18:1996/A1:2000&lt;br /&gt;
* IEC 60601-2-18:1996/A1:2000&lt;br /&gt;
* EN 60601-2-19:2009Medical electrical equipment - Part 2-19: Particular requirements for the basic safety and essential performance of infant incubators&lt;br /&gt;
* IEC 60601&lt;br /&gt;
* IEC 60601-2-19:2009	&lt;br /&gt;
* EN 60601-2-20:2009Medical electrical equipment - Part 2-20: Particular requirements for the basic safety and essential performance of infant transport incubators&lt;br /&gt;
* IEC 60601&lt;br /&gt;
* IEC 60601-2-20:2009	&lt;br /&gt;
* EN 60601-2-21:2009Medical electrical equipment - Part 2-21: Particular requirements for the basic safety and essential performance of infant radiant warmers&lt;br /&gt;
* IEC 60601-2-21:2009	&lt;br /&gt;
* EN 60601-2-22:1996Medical electrical equipment - Part 2: Particular requirements for the safety of diagnostic and therapeutic laser equipment&lt;br /&gt;
* IEC 60601-2-22:1995	&lt;br /&gt;
* EN 60601-2-23:2000Medical electrical equipment - Part 2-23: Particular requirements for the safety, including essential performance, of transcutaneous partial pressure monitoring equipment&lt;br /&gt;
* IEC 60601-2-23:1999	&lt;br /&gt;
* EN 60601-2-24:1998Medical electrical equipment - Part 2-24: Particular requirements for the safety of infusion pumps and controllers&lt;br /&gt;
* IEC 60601-2-24:1998	&lt;br /&gt;
* EN 60601-2-25:1995Medical electrical equipment - Part 2-25: Particular requirements for the safety of electrocardiographs&lt;br /&gt;
* IEC 60601-2-25:1993	&lt;br /&gt;
* EN 60601-2-25:1995/A1:1999&lt;br /&gt;
* IEC 60601-2-25:1993/A1:1999&lt;br /&gt;
* EN 60601-2-26:2003Medical electrical equipment - Part 2-26: Particular requirements for the safety of electroencephalographs&lt;br /&gt;
* IEC 60601-2-26:2002	&lt;br /&gt;
* EN 60601-2-27:2006Medical electrical equipment - Part 2-27: Particular requirements for the safety, including essential performance, of electrocardiographic monitoring equipment&lt;br /&gt;
* IEC 60601-2-27:2005	&lt;br /&gt;
* EN 60601-2-27:2006/AC:2006&lt;br /&gt;
* EN 60601-2-28:2010Medical electrical equipment - Part 2-28: Particular requirements for the basic safety and essential performance of X-ray tube assemblies for medical diagnosis&lt;br /&gt;
* IEC 60601-2-28:2010	&lt;br /&gt;
* EN 60601-2-29:2008Medical electrical equipment - Part 2-29: Particular requirements for the basic safety and essential performance of radiotherapy simulators&lt;br /&gt;
* IEC 60601-2-29:2008	&lt;br /&gt;
* EN 60601-2-30:2000Medical electrical equipment -- Part 2-30: Particular requirements for the safety, including essential performance, of automatic cycling non-invasive blood pressure monitoring equipment&lt;br /&gt;
* IEC 60601-2-30:1999	&lt;br /&gt;
* EN 60601-2-33:2010 (new)Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis&lt;br /&gt;
* IEC 60601&lt;br /&gt;
* IEC 60601-2-33:2010	&lt;br /&gt;
* EN 60601-2-33:2010/A1:2015&lt;br /&gt;
* IEC 60601-2-33:2010/A1:2013 (new)&lt;br /&gt;
* EN 60601-2-33:2010/A2:2015&lt;br /&gt;
* IEC 60601-2-33:2010/A2:2015 (new)&lt;br /&gt;
* EN 60601-2-33:2010/AC:2016-03 (new)&lt;br /&gt;
* EN 60601-2-33:2010/A12:2016 (new)&lt;br /&gt;
* EN 60601-2-34:2000Medical electrical equipment - Part 2-34: Particular requirements for the safety, including essential performance, of invasive blood pressure monitoring equipment&lt;br /&gt;
* IEC 60601-2-34:2000	&lt;br /&gt;
* EN 60601-2-36:1997Medical electrical equipment - Part 2: Particular requirements for the safety of equipment for extracorporeally induced lithotripsy&lt;br /&gt;
* IEC 60601-2-36:1997	&lt;br /&gt;
* EN 60601-2-37:2008Medical electrical equipment - Part 2-37: Particular requirements for the basic safety and essential performance of ultrasonic medical diagnostic and monitoring equipment&lt;br /&gt;
* IEC 60601-2-37:2007	&lt;br /&gt;
* EN 60601-2-39:2008Medical electrical equipment - Part 2-39: Particular requirements for basic safety and essential performance of peritoneal dialysis equipment&lt;br /&gt;
* IEC 60601-2-39:2007	&lt;br /&gt;
* EN 60601-2-40:1998Medical electrical equipment - Part 2-40: Particular requirements for the safety of electromyographs and evoked response equipment&lt;br /&gt;
* IEC 60601-2-40:1998	&lt;br /&gt;
* EN 60601-2-41:2009Medical electrical equipment - Part 2-41: Particular requirements for basic safety and essential performance of surgical luminaires and luminaires for diagnosis&lt;br /&gt;
* IEC 60601-2-41:2009	&lt;br /&gt;
* EN 60601-2-43:2010Medical electrical equipment - Part 2-43: Particular requirements for basic safety and essential performance of X-ray equipment for interventional procedures&lt;br /&gt;
* IEC 60601-2-43:2010	&lt;br /&gt;
* EN 60601-2-44:2009Medical electrical equipment - Part 2-44: Particular requirements for the basic safety and essential performance of X-ray equipment for computed tomography&lt;br /&gt;
* IEC 60601-2-44:2009	&lt;br /&gt;
* EN 60601-2-45:2001Medical electrical equipment -- Part 2-45: Particular requirements for the safety of mammographic X-ray equipment and mammographic stereotactic devices&lt;br /&gt;
* IEC 60601-2-45:2001	&lt;br /&gt;
* EN 60601-2-46:1998Medical electrical equipment -- Part 2-46: Particular requirements for the safety of operating tables&lt;br /&gt;
* IEC 60601-2-46:1998	&lt;br /&gt;
* EN 60601-2-47:2001Medical electrical equipment - Part 2-47: Particular requirements for the safety, including essential performance, of ambulatory electrocardiographic systems&lt;br /&gt;
* IEC 60601-2-47:2001	&lt;br /&gt;
* EN 60601-2-49:2001Medical electrical equipment - Part 2-49: Particular requirements for the safety of multifunction patient monitoring equipment&lt;br /&gt;
* IEC 60601-2-49:2001	&lt;br /&gt;
* EN 60601-2-50:2009Medical electrical equipment - Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipment&lt;br /&gt;
* IEC 60601-2-50:2009	&lt;br /&gt;
* EN 60601-2-51:2003Medical electrical equipment - Part 2-51: Particular requirements for safety, including essential performance, of recording and analysing single channel and multichannel electrocardiographs&lt;br /&gt;
* IEC 60601-2-51:2003	&lt;br /&gt;
* EN 60601-2-52:2010Medical electrical equipment - Part 2-52: Particular requirements for basic safety and essential performance of medical beds (IEC 60601-2-52:2009)	&lt;br /&gt;
* EN 60601-2-52:2010/AC:2011&lt;br /&gt;
* EN 60601-2-54:2009Medical electrical equipment - Part 2-54: Particular requirements for the basic safety and essential performance of X-ray equipment for radiography and radioscopy&lt;br /&gt;
* IEC 60601-2-54:2009	&lt;br /&gt;
* EN 60627:2001Diagnostic X-ray imaging equipment - Characteristics of general purpose and mammographic anti-scatter grids&lt;br /&gt;
* IEC 60627:2001	&lt;br /&gt;
* EN 60627:2001/AC:2002&lt;br /&gt;
* EN 60645-1:2001Electroacoustics - Audiological equipment - Part 1: Pure-tone audiometers&lt;br /&gt;
* IEC 60645-1:2001	&lt;br /&gt;
* EN 60645-2:1997Audiometers - Part 2: Equipment for speech audiometry&lt;br /&gt;
* IEC 60645-2:1993&lt;br /&gt;
* EN 60645-3:2007Electroacoustics - Audiometric equipment - Part 3: Test signals of short duration&lt;br /&gt;
* IEC 60645-3:2007&lt;br /&gt;
* EN 60645-4:1995Audiometers - Part 4: Equipment for extended high-frequency audiometry&lt;br /&gt;
* IEC 60645-4:1994&lt;br /&gt;
* EN 61217:2012Radiotherapy equipment - Coordinates, movements and scales&lt;br /&gt;
* IEC 61217:2011	&lt;br /&gt;
* EN 61676:2002Medical electrical equipment - Dosimetric instruments used for non-invasive measurement of X-ray tube voltage in diagnostic radiology&lt;br /&gt;
* IEC 61676:2002&lt;br /&gt;
* EN 61676:2002/A1:2009&lt;br /&gt;
* IEC 61676:2002/A1:2008&lt;br /&gt;
* EN 62083:2009Medical electrical equipment - Requirements for the safety of radiotherapy treatment planning systems&lt;br /&gt;
* IEC 62083:2009&lt;br /&gt;
* EN 62220-1:2004Medical electrical equipment - Characteristics of digital X-ray imaging devices - Part 1: Determination of the detective quantum efficiency&lt;br /&gt;
* IEC 62220-1:2003	&lt;br /&gt;
* EN 62220-1-2:2007Medical electrical equipment - Characteristics of digital X-ray imaging devices - Part 1-2: Determination of the detective quantum efficiency - Detectors used in mammography&lt;br /&gt;
* IEC 62220-1-2:2007	&lt;br /&gt;
* EN 62220-1-3:2008Medical electrical equipment - Characteristics of digital X-ray imaging devices - Part 1-3: Determination of the detective quantum efficiency - Detectors used in dynamic imaging&lt;br /&gt;
* IEC 62220-1-3:2008	&lt;br /&gt;
* EN 62304:2006Medical device software - Software life-cycle processes&lt;br /&gt;
* IEC 62304:2006	&lt;br /&gt;
* EN 62304:2006/AC:2008&lt;br /&gt;
* EN 62366:2008Medical devices - Application of usability engineering to medical devices&lt;br /&gt;
* IEC 62366:2007	&lt;br /&gt;
* EN 80601-2-35:2009Medical electrical equipment - Part 2-35: Particular requirements for the basic safety and essential performance of heating devices using blankets, pads and mattresses and intended for heating in medical use&lt;br /&gt;
* IEC 80601-2-35:2009	&lt;br /&gt;
* EN 80601-2-58:2009Medical electrical equipment - Part 2-58: Particular requirements for the basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery&lt;br /&gt;
* IEC 80601-2-58:2008	&lt;br /&gt;
* EN 80601-2-59:2009Medical electrical equipment - Part 2-59: Particular requirements for the basic safety and essential performance of screening thermographs for human febrile temperature screening&lt;br /&gt;
* IEC 80601&lt;br /&gt;
* IEC 80601-2-59:2008	&lt;br /&gt;
&lt;br /&gt;
Base: Council Directive 93/42/EEC of 14 June 1993 concerning medical devices OJ L 169 of 12 July 1993&lt;br /&gt;
&lt;br /&gt;
MDD是欧盟医疗器械93/42/EEC指令的简称，适用于在欧盟国家销售的医疗器械进行认证，是强制认证，需要由获得授权的公告机构进行认证。&lt;br /&gt;
&lt;br /&gt;
MDD指令的产品分3个等级：一类，二类，三类，危险等级越高的产品划分的等级越高，认证就越严格，周期越长，费用越高。&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E5%AE%B6%E7%94%B5CE%E8%AE%A4%E8%AF%81&amp;diff=132</id>
		<title>家电CE认证</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E5%AE%B6%E7%94%B5CE%E8%AE%A4%E8%AF%81&amp;diff=132"/>
		<updated>2019-07-15T09:52:57Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&#039;&#039;&#039;EMC标准&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
  EN55014-1&lt;br /&gt;
  EN55014-2&lt;br /&gt;
  EN 61000-3-2&lt;br /&gt;
  EN 61000-3-3&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;LVD标准&#039;&#039;&#039;&lt;br /&gt;
  EN 60335-x-x（看看要做的家电产品适用哪个？）详细参阅[[IEC60335]] https://www.emc.wiki/html/IEC60335&lt;br /&gt;
  EN 60335-1:2012/A14:2019 &lt;br /&gt;
  EN 62233:2008&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;如果另外还带WIFI，那么必须还需要满足&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;RED标准&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
  EN 300 328 Ver. 2.1.1&lt;br /&gt;
  EN 301 489-1 Ver. 2.1.1  &lt;br /&gt;
  EN 301 489-17 Ver. 3.1.1&lt;br /&gt;
  EN 62311&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;如果另外还带BT，那么必须还需要满足&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;RED标准&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
  EN 300 328 Ver. 2.1.1&lt;br /&gt;
  EN 301 489-1 Ver. 2.1.1  &lt;br /&gt;
  EN 301 489-17 Ver. 3.1.1&lt;br /&gt;
  EN 62479&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E7%94%B5%E7%A3%81%E5%85%BC%E5%AE%B9%E4%B8%89%E8%A6%81%E7%B4%A0&amp;diff=164</id>
		<title>电磁兼容三要素</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E7%94%B5%E7%A3%81%E5%85%BC%E5%AE%B9%E4%B8%89%E8%A6%81%E7%B4%A0&amp;diff=164"/>
		<updated>2019-07-14T14:09:55Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; 什么是电磁兼容三要素？&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;骚扰源&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
dv/dt and di/dt 突变的电压电流产生电磁干扰&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;耦合途径&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
任何等效导线、PCB trace、机壳等&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;敏感设备&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
敏感电路、敏感的小信号等&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=EMC%E8%A7%84%E5%BE%8B&amp;diff=52</id>
		<title>EMC规律</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=EMC%E8%A7%84%E5%BE%8B&amp;diff=52"/>
		<updated>2019-07-14T14:08:21Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&#039;&#039;&#039;EMC三个重要规律&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;&#039;&#039;规律一&#039;&#039;&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
EMC费效比关系规律： EMC问题越早考虑、越早解决，费用越小、效果越好。&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;&#039;&#039;规律二&#039;&#039;&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
高频电流环路面积S越大, EMI辐射越严重。&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;&#039;&#039;规律三&#039;&#039;&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
环路电流频率F越高，引起的EMI辐射越严重，电磁辐射场强随电流频率f的平方成正比增大。&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E8%88%9E%E5%8F%B0%E7%81%AFCE%E8%AE%A4%E8%AF%81&amp;diff=174</id>
		<title>舞台灯CE认证</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E8%88%9E%E5%8F%B0%E7%81%AFCE%E8%AE%A4%E8%AF%81&amp;diff=174"/>
		<updated>2019-07-12T16:37:45Z</updated>

		<summary type="html">&lt;p&gt;EMC：​创建页面，内容为“舞台灯做CE认证，需要做什么标准呢？  &amp;#039;&amp;#039;&amp;#039;CE-EMC电磁兼容标准&amp;#039;&amp;#039;&amp;#039; * EN 55032:2015+ AC:2016 多媒体设备的电磁兼容性 - 发射要求 * EN 551…”&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;舞台灯做CE认证，需要做什么标准呢？&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;CE-EMC电磁兼容标准&#039;&#039;&#039;&lt;br /&gt;
* EN 55032:2015+ AC:2016 多媒体设备的电磁兼容性 - 发射要求&lt;br /&gt;
* EN 55103-2:2009+IS1:2012 电磁兼容性 专业用音频，视频，视听和娱乐照明控制设备的产品系列标准。 第2部分：抗扰度&lt;br /&gt;
* EN 61000-3-2:2014 谐波&lt;br /&gt;
* EN 61000-3-3:2013 闪烁&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;CE-LVD安规标准&#039;&#039;&#039;&lt;br /&gt;
* EN 60598-1 灯具通用安全要求&lt;br /&gt;
* EN 60598-2-17 灯具 第2部分：特殊要求 第17节：舞台照明、电视、电影和摄影场所（室内外）用灯具　&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E9%81%A5%E6%8E%A7%E5%99%A8%E5%8A%A0%E6%8B%BF%E5%A4%A7IC-ID&amp;diff=178</id>
		<title>遥控器加拿大IC-ID</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E9%81%A5%E6%8E%A7%E5%99%A8%E5%8A%A0%E6%8B%BF%E5%A4%A7IC-ID&amp;diff=178"/>
		<updated>2019-07-12T16:27:55Z</updated>

		<summary type="html">&lt;p&gt;EMC：​创建页面，内容为“* RSS-Gen Issue 5 March 2019 Amendment 1 无线电设备合规性的一般要求 * RSS-210 Issue 9 August 2016 Amendment November 2017 免许可证无线电设备：…”&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;* RSS-Gen Issue 5 March 2019 Amendment 1 无线电设备合规性的一般要求&lt;br /&gt;
* RSS-210 Issue 9 August 2016 Amendment November 2017 免许可证无线电设备：I类设备&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
 RSS-Gen — General Requirements for Compliance of Radio Apparatus&lt;br /&gt;
* 内容&lt;br /&gt;
* 范围 &lt;br /&gt;
* 1.1         过渡期&lt;br /&gt;
* 概述 &lt;br /&gt;
* 2.1         目的和应用 &lt;br /&gt;
* 2.2         与无线电标准规范 有关的查询&lt;br /&gt;
* 2.3         与许可有关的查询 &lt;br /&gt;
* 2.4         认证机构 &lt;br /&gt;
* 2.5         适用RSS的过渡期 &lt;br /&gt;
* 2.6         无线电设备的类别 &lt;br /&gt;
* 2.7         除外 &lt;br /&gt;
* 2.8         用于发展目的的 无线电设备&lt;br /&gt;
* 2.9         特别授权所涵盖的无线电设备 &lt;br /&gt;
* 2.10       确定干扰&lt;br /&gt;
* 规范性出版物和相关文件 &lt;br /&gt;
* 3.1         概述 &lt;br /&gt;
* 3.2         测量方法，测量仪器和测试现场验证 &lt;br /&gt;
* 3.3         无线电标准程序RSP-100 &lt;br /&gt;
* 3.4         无线电频率接触符合性 &lt;br /&gt;
* 3.5         无线电通信天线系统 &lt;br /&gt;
* 3.6         其他相关文件&lt;br /&gt;
* 标签要求 &lt;br /&gt;
* 4.1         总则 &lt;br /&gt;
* 4.2         认证产品的标签 &lt;br /&gt;
* 4.3         模块（第I类）和主机产品标签要求 &lt;br /&gt;
* 4.4         电子标签（电子标签）&lt;br /&gt;
* 接收器 &lt;br /&gt;
* 5.1         扫描器接收器 &lt;br /&gt;
* 5.2         在30-960 MHz频段工作的独立接收器 &lt;br /&gt;
* 5.3         其他接收器&lt;br /&gt;
* 一般管理和技术要求 &lt;br /&gt;
* 6.1         辅助设备和附件 &lt;br /&gt;
* 6.2         测试实验室要求 &lt;br /&gt;
* 6.3         测试报告 &lt;br /&gt;
* 6.4         外部控制 &lt;br /&gt;
* 6.5         频率低于30 MHz的近场测量方法 &lt;br /&gt;
* 6.6         频率高于30 MHz的测量距离 &lt;br /&gt;
* 6.7         占用带宽（或99％发射带宽）和x dB带宽 &lt;br /&gt;
* 6.8         发射天线 &lt;br /&gt;
* 6.9         工作频段和测试频率的选择 &lt;br /&gt;
* 6.10       CISPR准峰值和CISPR平均值检测器 &lt;br /&gt;
* 6.11       发射机频率稳定性 &lt;br /&gt;
* 6.12       发射机输出功率 &lt;br /&gt;
* 6.13       发射机无用发射&lt;br /&gt;
* 接收机发射限值 &lt;br /&gt;
* 7.1         概述 &lt;br /&gt;
* 7.2         交流电力线传导发射限值 &lt;br /&gt;
* 7.3         接收机辐射发射限值 &lt;br /&gt;
* 7.4         接收机传导发射限值&lt;br /&gt;
* 免许可证无线电设备 &lt;br /&gt;
* 8.1         测量带宽和探测器功能 &lt;br /&gt;
* 8.2         脉冲操作 &lt;br /&gt;
* 8.3         放大器禁止 &lt;br /&gt;
* 8.4         用户手册注意 &lt;br /&gt;
* 8.5         现场（现场）免许可设备的测量 &lt;br /&gt;
* 8.6         主/从网络中设备的工作频率范围 &lt;br /&gt;
* 8.7         无线电频率识别（RFID）设备 &lt;br /&gt;
* 8.8         交流电力线传导发射限值 &lt;br /&gt;
* 8.9         发射机发射限值 &lt;br /&gt;
* 8.10       限制频段 &lt;br /&gt;
* 8.11       频率稳定性&lt;br /&gt;
* 常用RSS术语和定义词汇表&lt;br /&gt;
* 附件A（规范性）       测试报告内容&lt;br /&gt;
* 附件B（规范性附录）       电子标签（电子标签）要求&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
 RSS-210 — Licence-Exempt Radio Apparatus: Category I Equipment&lt;br /&gt;
* 内容&lt;br /&gt;
* 1.  范围&lt;br /&gt;
* 2. 一般信息&lt;br /&gt;
* 2.1  许可要求&lt;br /&gt;
* 2.2  相关文件&lt;br /&gt;
* 3.  一般要求&lt;br /&gt;
* 3.1  RSS-Gen合规性&lt;br /&gt;
* 4.  技术规格&lt;br /&gt;
* 4.1 限制频段内的辐射&lt;br /&gt;
* 4.2 无绳电话（一般条件）&lt;br /&gt;
* 4.3  一般场强限制&lt;br /&gt;
* 4.4  具有通用场强限制范围内的通用排放的变送器。&lt;br /&gt;
* 附件A - 瞬时操作设备和遥控器&lt;br /&gt;
* 附件B - 适用于任何应用的频带工作设备&lt;br /&gt;
* 附件C - 医疗遥测，无线麦克风，听觉辅助，货物追踪和执法&lt;br /&gt;
* 附件D - 433.5-434.5 MHz频段内的射频识别（RFID）设备&lt;br /&gt;
* 附件E - 家庭无线电服务（FRS），通用移动无线电业务（GMRS）和通用移动无线电业务-M（GMRS-M）&lt;br /&gt;
* 附件F - 工作在902-928 MHz，2435-2465 MHz，5785-5815 MHz，10.5-10.55 GHz，24.075-24.175 GHz和33.4-36 GHz频段的设备&lt;br /&gt;
* 附件G - 在电视频段工作的低功率无线电设备&lt;br /&gt;
* 附件H - 车辆识别&lt;br /&gt;
* 附件I - 24.05-24.25 GHz频段内的固定点对点系统&lt;br /&gt;
* 附件J - 工作在57-64 GHz频段的设备&lt;br /&gt;
* 附件K - 在5925-7250 MHz频段内工作的宽带设备&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E7%BE%8E%E5%9B%BDWIFI%E8%AE%A4%E8%AF%81&amp;diff=172</id>
		<title>美国WIFI认证</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E7%BE%8E%E5%9B%BDWIFI%E8%AE%A4%E8%AF%81&amp;diff=172"/>
		<updated>2019-07-12T02:09:27Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;美国 FCC 47CFR Part 15: Subpart C Section 15.247&lt;br /&gt;
加拿大IC RSS-247&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;TEST SUMMARY&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
5.1.1 ANTENNA REQUIREMENT&lt;br /&gt;
&lt;br /&gt;
5.1.2 PEAK OUTPUT POWER&lt;br /&gt;
&lt;br /&gt;
5.1.3 6DB BANDWIDTH AND 99%BANDWIDTH&lt;br /&gt;
&lt;br /&gt;
5.1.4 POWER DENSITY&lt;br /&gt;
&lt;br /&gt;
5.1.5 CONDUCTED SPURIOUS EMISSIONS AND FREQUENCY BAND EDGE MEASURED IN 100KHZ BANDWIDTH&lt;br /&gt;
&lt;br /&gt;
5.1.6 SPURIOUS EMISSION&lt;br /&gt;
&lt;br /&gt;
5.2.1 MAINS CONDUCTED EMISSIONS&lt;br /&gt;
&lt;br /&gt;
6.1.1 ELECTROMAGNETIC FIELDS&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Safety Human exposure&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
Radio Frequency Exposure Compliance&lt;br /&gt;
&lt;br /&gt;
Test standard : FCC KDB Publication 447498 D01 v06 RSS 102&lt;br /&gt;
&lt;br /&gt;
Separation distance is more than 20 cm, thus mobile device exposure limits can be applied.&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E6%AC%A7%E6%B4%B2WIFI%E8%AE%A4%E8%AF%81&amp;diff=156</id>
		<title>欧洲WIFI认证</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E6%AC%A7%E6%B4%B2WIFI%E8%AE%A4%E8%AF%81&amp;diff=156"/>
		<updated>2019-07-12T02:05:43Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;WIFI广泛应用在各类电子电器产品实现各种无线控制功能，实现科技方便人们的生活。&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;RED射频RF标准&#039;&#039;&#039;&lt;br /&gt;
 EN 300 328 Ver. 2.1.1&lt;br /&gt;
 EN 301 489-1 Ver. 2.1.1  &lt;br /&gt;
 EN 301 489-17 Ver. 3.1.1&lt;br /&gt;
 EN 62311&lt;br /&gt;
&lt;br /&gt;
如果嵌入在某类型产品里面，则需要满足相对应的产品标准，例如多媒体产品则需要满足：&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EMC标准&#039;&#039;&#039;&lt;br /&gt;
 EN 61000-3-2&lt;br /&gt;
 EN 61000-3-3&lt;br /&gt;
 EN 55032&lt;br /&gt;
 EN 55035 or EN 55024&lt;br /&gt;
&lt;br /&gt;
同样还有与之对应的LVD安规标准，例如多媒体产品则需要满足：&lt;br /&gt;
EN 62368&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;TEST SUMMARY&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
* 4.1.1 RF OUTPUT POWER&lt;br /&gt;
&lt;br /&gt;
* 4.1.2 MAXIMUM SPECTRAL POWER DENSITY&lt;br /&gt;
&lt;br /&gt;
* 4.1.3 DUTY CYCLE, TX-SEQUENCE, TX-GAP&lt;br /&gt;
&lt;br /&gt;
* 4.1.4 MEDIUM UTILISATION FACTOR&lt;br /&gt;
&lt;br /&gt;
* 4.1.5 ADAPTIVITY&lt;br /&gt;
&lt;br /&gt;
* 4.1.6 OCCUPIED CHANNEL BANDWIDTH&lt;br /&gt;
&lt;br /&gt;
* 4.1.7 TRANSMITTER UNWANTED EMISSIONS IN THE OOB DOMAIN&lt;br /&gt;
&lt;br /&gt;
* 4.1.8 TRANSMITTER UNWANTED EMISSIONS IN THE SPURIOUS DOMAIN&lt;br /&gt;
&lt;br /&gt;
* 4.2.1 RECEIVER RADIATED SPURIOUS EMISSIONS&lt;br /&gt;
&lt;br /&gt;
* 4.2.2 RECEIVER BLOCKING&lt;br /&gt;
&lt;br /&gt;
* 4.2.3 GEO-LOCATION CAPABILITY&lt;br /&gt;
&lt;br /&gt;
* 5.1.1 ELECTROMAGNETIC FIELDS&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E6%B0%B4%E6%97%8F%E9%A6%86%E8%BF%87%E6%BB%A4%E5%99%A8CE%E8%AE%A4%E8%AF%81&amp;diff=158</id>
		<title>水族馆过滤器CE认证</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E6%B0%B4%E6%97%8F%E9%A6%86%E8%BF%87%E6%BB%A4%E5%99%A8CE%E8%AE%A4%E8%AF%81&amp;diff=158"/>
		<updated>2019-07-11T15:02:27Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;水族馆过滤器若是普通例如由电机、控制电路、管道等没有任何无线RF射频相关，则做EMC、LVD即可，如果内置有如WIFI无线控制模块实现某些控制功能的话，则需要满足RED指令标准。另外，如果有外置适配器的话，那么外置电源就还需要满足安规标准EN 60335-1 or EN 61558-2-16，否则外置电源就还需要做随机测试。&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EMC标准&#039;&#039;&#039;&lt;br /&gt;
  EN55014-1&lt;br /&gt;
  EN55014-2&lt;br /&gt;
  EN 61000-3-2&lt;br /&gt;
  EN 61000-3-3&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;LVD标准&#039;&#039;&#039;&lt;br /&gt;
  EN 60335-2-55:2003/A11:2018 &lt;br /&gt;
  EN 60335-1:2012/A14:2019 &lt;br /&gt;
  EN 62233:2008&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;RED标准&#039;&#039;&#039;&lt;br /&gt;
  EN 300 328 Ver. 2.1.1&lt;br /&gt;
  EN 301 489-1 Ver. 2.1.1  &lt;br /&gt;
  EN 301 489-17 Ver. 3.1.1&lt;br /&gt;
  EN 62311&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=FCC%E8%AE%A4%E8%AF%81%E9%9C%80%E8%A6%81%E8%B5%84%E6%96%99&amp;diff=68</id>
		<title>FCC认证需要资料</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=FCC%E8%AE%A4%E8%AF%81%E9%9C%80%E8%A6%81%E8%B5%84%E6%96%99&amp;diff=68"/>
		<updated>2019-07-11T03:20:10Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; FCC认证需要资料分两种，一种是FCC SDOC、一种是FCC ID。&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;FCC SDOC认证&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
FCC SDOC认证，是指出口美国的归属且不限于FCC PART 15、FCC PART 18的所有的且产品内部没有任何有意发射的射频模块以及电路，既无意发射的电子电器产品。例如，普通开关电源、普通显示器、普通打印机有线鼠标、键盘、SSD硬盘等等。&lt;br /&gt;
&lt;br /&gt;
 这类提供产品1套、认证的申请表即可，这种比较简单。&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;FCC ID认证&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
FCC ID认证，是指那些出口美国的归属且不限于FCC PART 15C的所有的且内部具有相关射频发射模块以及电路，既具有意发射的电子电器产品。例如，采用zigbee\WIFI\BT技术的各类产品，各类无线遥控器、手机等。&lt;br /&gt;
&lt;br /&gt;
 这类提供产品需要提供一共至少2台样机，普通的样机一台、可以进行定频RF射频测试的样机一台，需要的资料也多，详细如下列表：&lt;br /&gt;
&lt;br /&gt;
* 申请表&lt;br /&gt;
* FCC官网账号密码（不限于FCC的注册号码FRN、FCC的Grantee Code（授权码）公司代号）&lt;br /&gt;
* FCC label 位置及其规格（铭牌） 必须标明大小尺寸，以及在产品上的位置。 FCC label须包含 FCC ID号和 FCC警语，如果 label尺寸小，可只标明 FCC ID号，但 FCC警语一定要写在使用手册中（用户说明书）。其它如生产商，产品名称型号等信息可自行决定是否写在 label中。&lt;br /&gt;
* 产品简要描述文档，关于工作原理、功能描述、请对产品的功能、用途、信号流程、各功能电路相互关系，电源供电做一个简短的说明&lt;br /&gt;
* 电路方框图（必须标明电路中所用到的任何晶振频率）&lt;br /&gt;
* 电路原理图（请确保清晰，其位号也需要看得清）&lt;br /&gt;
* 天线增益&lt;br /&gt;
* 用户手册或使用说明书&lt;br /&gt;
* 授权信&lt;br /&gt;
* 保密信(如需要保密)&lt;br /&gt;
* 定频方法以及必要的辅助硬件与软件&lt;br /&gt;
* RF模块规格书，其中信息包括且不限于调制方式、功率频率频道列表、功率、带宽、天线安装方式、是否多模、是否多制式兼容等信息。&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E9%9F%A9%E5%9B%BD%E7%81%AF%E5%85%B7EMC%E6%A0%87%E5%87%86&amp;diff=184</id>
		<title>韩国灯具EMC标准</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E9%9F%A9%E5%9B%BD%E7%81%AF%E5%85%B7EMC%E6%A0%87%E5%87%86&amp;diff=184"/>
		<updated>2019-07-10T10:40:42Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; 韩国灯具EMC标准&lt;br /&gt;
&lt;br /&gt;
LED灯具、驱动器卖去韩国EMC需要做什么测试呢？&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;KN 15 / CISPR 15&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
* 9k-30M 传导&lt;br /&gt;
* 9k-30M 辐射&lt;br /&gt;
* 30M-300M 辐射&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
如果是LED驱动器认证，那么必须配LED灯板进行模拟测试，而不能用电阻负载替代。&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E6%BE%B3%E6%B4%B2%E7%81%AF%E5%85%B7EMC%E6%A0%87%E5%87%86&amp;diff=162</id>
		<title>澳洲灯具EMC标准</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E6%BE%B3%E6%B4%B2%E7%81%AF%E5%85%B7EMC%E6%A0%87%E5%87%86&amp;diff=162"/>
		<updated>2019-07-10T10:32:06Z</updated>

		<summary type="html">&lt;p&gt;EMC：​创建页面，内容为“ &amp;#039;&amp;#039;&amp;#039;澳洲灯具EMC标准&amp;#039;&amp;#039;&amp;#039;  LED灯具、驱动器卖去澳洲EMC需要做什么测试呢？   &amp;#039;&amp;#039;&amp;#039;AS/NZS CISPR15&amp;#039;&amp;#039;&amp;#039;   * 9k-30M 传导  * 9k-30M 辐射  * 30M-300M…”&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; &#039;&#039;&#039;澳洲灯具EMC标准&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
LED灯具、驱动器卖去澳洲EMC需要做什么测试呢？&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;AS/NZS CISPR15&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
* 9k-30M 传导&lt;br /&gt;
&lt;br /&gt;
* 9k-30M 辐射&lt;br /&gt;
&lt;br /&gt;
* 30M-300M 辐射&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
如果是LED驱动器认证，那么必须配LED灯板进行模拟测试，而不能用电阻负载替代。&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E6%97%A5%E6%9C%AC%E7%81%AF%E5%85%B7EMC%E6%A0%87%E5%87%86&amp;diff=146</id>
		<title>日本灯具EMC标准</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E6%97%A5%E6%9C%AC%E7%81%AF%E5%85%B7EMC%E6%A0%87%E5%87%86&amp;diff=146"/>
		<updated>2019-07-10T10:27:50Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt; &#039;&#039;&#039;日本灯具EMC标准&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
LED灯具、驱动器卖去日本EMC需要做什么测试呢？&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;J55015&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
* 传导&lt;br /&gt;
&lt;br /&gt;
* 9k-30M辐射&lt;br /&gt;
&lt;br /&gt;
* 30M-300M辐射&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
如果是LED驱动器认证，那么必须配LED灯板进行模拟测试，否则按照电源适配器的要求进行满载、半载、空载等要求进行评估测试。&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E5%B9%B2%E6%89%8B%E6%9C%BACE%E8%AE%A4%E8%AF%81&amp;diff=134</id>
		<title>干手机CE认证</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E5%B9%B2%E6%89%8B%E6%9C%BACE%E8%AE%A4%E8%AF%81&amp;diff=134"/>
		<updated>2019-07-09T03:59:21Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;干手机HandDryer卖去欧洲需要满足什么标准呢？&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;EMC&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
IEC/EN 61000-3-2&lt;br /&gt;
IEC/EN 61000-3-3&lt;br /&gt;
CISPR 14-1 / EN 55014-1&lt;br /&gt;
CISPR 14-2 / EN 55014-1&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Safety&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
IEC / EN 60335-1&lt;br /&gt;
IEC / EN 60335-2-23&lt;br /&gt;
IEC / EN 62233&lt;br /&gt;
&lt;br /&gt;
如果是卖去海湾七国例如做做Gmark用IEC报告的话，那么IEC / EN 62233就不用做了，满足IEC / EN 60335-1与IEC / EN 60335-2-23即可。&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E5%8D%B0%E5%BA%A6WPC&amp;diff=128</id>
		<title>印度WPC</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E5%8D%B0%E5%BA%A6WPC&amp;diff=128"/>
		<updated>2019-07-06T07:47:31Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&#039;&#039;&#039;印度WPC认证简介&#039;&#039;&#039;&lt;br /&gt;
印度 WPC (Wireless Planning &amp;amp; Coordination Wing)是印度管制无线法规的机构，所有无线产品在进入市场之前必须取得WPC的核准。印度无线通讯产品依据产品类型分别由无线规划与协调部（WPC）和通讯工程中心（TEC）两个管制机构分别管控。印度的频段有分免费开放和暂未开放两类。针对免费开放的频段，此类设备只需申请ETA（equipment type approval）证书；而其他未免费开放的频段，则需要申请执照。ETA 和执照的持有人都必须是当地注册的公司。基于CE R&amp;amp;TTE 或者 FCC ID (印度当地标准)&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
根据印度WPC 2019年2月26日公布的备忘录，欧洲技术认可ETA(European Technical Approval)认证对于使用豁免频段的低功率产品将豁免（例如使用蓝牙，NFC等的产品）。&lt;br /&gt;
&lt;br /&gt;
印度当地进口商/代理公司使用RF测试报告、支付WPC费用以及提供相关出货信息来申请自我宣称（SDOC）即可进行清关。&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;WPC SDOC申请流程&#039;&#039;&#039;&lt;br /&gt;
	&lt;br /&gt;
* 1）在www.wpc.dot.gov.in中在适当的类别中在线提交许可证申请，而不必跳过任何步骤&lt;br /&gt;
* 2）在线填写后，阅读提供的清单。&lt;br /&gt;
* 3）在线填写后，从应用程序ID中打印出来。&lt;br /&gt;
* 4）根据具体情况，向WPC办公室/ RLO提交相关申请表的硬拷贝以及打印出的应用程序ID副本。&lt;br /&gt;
* 5）按照WPC的后续说明进行操作。密切关注网站上许可证申请的状态。&lt;br /&gt;
&lt;br /&gt;
* - 提供出货型号的RF测试报告，该报告需要有资质的实验室出具方可被接受；&lt;br /&gt;
* - 当地进口商或代理公司审核测试报告是否真实且无需更改；&lt;br /&gt;
* - 支付WPC费用；&lt;br /&gt;
* - 将测试报告、支付单据以及发货信息（预计出货日期）邮件发送至邮箱etaselfdecl.wpc-dot@gov.in&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;管制产品范围&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
 WPC&lt;br /&gt;
覆盖所有带有无线电发射装置的设备。无线局域网（WLAN）设备，如Wi-Fi设备、蓝牙设备、Zigbee设备、WiMAX设备、RFID设备、非接触式智能卡阅读器，并结合了一些其它的RF发射器的产品RF。&lt;br /&gt;
&lt;br /&gt;
 TEC&lt;br /&gt;
与公共网络或广域网（WAN）服务接口的通信或网络设备，其中包括移动（GSM、WCDMA、LTE、2g、3g、4g）手机。常见的电信网络接口包括T1/ E1、ISDN BRI、PRI ISDN、ADSL、串行和模拟PSTN等等。&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;法律法规及认证要求&#039;&#039;&#039;&lt;br /&gt;
 WPC&lt;br /&gt;
无线产品在印度无线认证可分为ETA（Equipment Type of Approval）认证和License执照两种模式，其判定依据来源于申请设备所使用的工作频段。对于免费开放的频段例如13.56 MHz、433MHz、2.4GHz、5.725-5.825 GHz等，需要申请ETA认证；如果设备使用其它非免费开放的频段，如GSM、WCDMA手机等，则需要申请执照。&lt;br /&gt;
&lt;br /&gt;
 对于ETA认证，印度认可欧洲标准，WPC通过审核报告的方式签署证书。而对于License执照，则需要满足印度的标准要求。&lt;br /&gt;
&lt;br /&gt;
 对于ETA申请，产品不需要送到印度当地进行测试，产品具有RED or FCC ID报告即可向WPC提交认可申请。&lt;br /&gt;
&lt;br /&gt;
 TEC&lt;br /&gt;
* 终端通讯产品TEC有几种认证形式，包括Interface Approval和Type Approval等。&lt;br /&gt;
* Interface Approval依据的是TEC发布的Interface Requirements (IR) standards，Type Approval依据的是TEC发布的Generic Requirements (GR) standards。&lt;br /&gt;
* 产品样品必须送到印度当地TEC认可的实验室去进行测试，产品通过测试后，实验室出具相关的测试报告，申请人取得报告之后向TEC提交认可申请。&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;认证须知&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
WPC和TEC的持证者必须是印度当地公司。&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;印度常见问题解答&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
http://www.wpc.dot.gov.in/faq.asp&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;印度WPC官方联系方式&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
mails.wpc@nic.in&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E7%BE%8E%E5%9B%BDFCC_ID&amp;diff=168</id>
		<title>美国FCC ID</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E7%BE%8E%E5%9B%BDFCC_ID&amp;diff=168"/>
		<updated>2019-07-06T03:15:08Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[文件:FCC.jpg|330x220px|无框]]&lt;br /&gt;
&lt;br /&gt;
 FCC标识符，FCC ID认证必须在铭牌上面打上已经获得认证的ID号码，例如：FCC ID AAAAAXXXXX，AAAAA 代表5位字符的厂商编码（Grantee Code），XXXXX 由不超过14位的数字、字母、中横杆字符组成，是申请人设备的唯一代码，中横杆-也算一位字符。&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;FCC ID&#039;&#039;&#039;（FCC CERTIFICATION认证证书）认证&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;主要针对产品包括&#039;&#039;&#039;&lt;br /&gt;
 无线射频产品，例如BT、Wifi、Zigbee、2.4GHz、5GHz、手机产品、各类遥控器等有意发射产品，均需要符合美国FCC PART 15C标准限值。&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;认证方式&#039;&#039;&#039;&lt;br /&gt;
 产品需通过FCC认可的测试室测试完毕，取得测试报告后，整理产品的技术资料，包括：产品细节照片、方块图、使用手册等，详细资料可参阅 https://iec.EMC.design/thread-2297-1-1.html。再由FCC 认可的测试实验室提交给FCC TCB测试室确认所有资料无误（或者直接找TCB），并颁发证书。&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;FCC ID基本申请流程&#039;&#039;&#039;&lt;br /&gt;
 &#039;&#039;&#039;在中国必须要找拥有NVLAP or A2LA美国认可的无线射频实验室申请&#039;&#039;&#039;&lt;br /&gt;
 申请FCC ID = Grantee Code + Product code（申请成功之后将会拥有这串号码）先申请一个 FRN ，用来填写其它的表格。如果申请人是第一次申请 FCC ID ，就需要申请一个永久性的 Grantee Code 。在等待FCC批准分发给申请人 Grantee Code 的同时，申请人应抓紧时间将设备进行检测。待准备好所有 FCC 要求提交的材料并且检测报告已经完成时， FCC 应该已经批准了 Grantee Code 。申请人用这个 Code 、检测报告和要求的材料在网上完成 FCC Form 731 和 Form 159 。 FCC 收到 Form 159 和汇款后，就开始受理认证的申请。受理结束时， FCC 会将 FCC ID 的 Original Grant 寄给申请人。申请人拿到证书后就可以出售或出口相应产品了。&lt;br /&gt;
&lt;br /&gt;
 需提供以下资料：&lt;br /&gt;
&lt;br /&gt;
*Applicant’s Product Name ,Model NO., Mailing Address , Phone No.,Fax No., Contact Person &amp;amp; His Title。申请方的名字，产品名，型号，地址，电话，邮件，传真，联系人及其职位。&lt;br /&gt;
&lt;br /&gt;
*For transmitter, the fundamental frequency(Operation within the bands)。针对发射部分，发射的基波频率(最好提供使用的频段)。&lt;br /&gt;
&lt;br /&gt;
*Applicant’s FCC Registration Number (FRN) 申请方的FCC的注册号码FRN（ FCC Registration Number），此为政府给予企业的身份识别号，可在FCC官方网站免费申请，在申请后由网站自动生成给企业，共10位数字由NPS Lab协助提供。申请认证方在申请FCC 认证注册时，由 FCC CORES 所发出的一个10 位数值参考代号。对于第一次申请FCC ID的客户可在 FCC 网站免费申请。详细参阅：FCC FRN注册号链接：https://fjallfoss.fcc.gov/coresWeb/publicHome.do&lt;br /&gt;
&lt;br /&gt;
*需要提供Grantee Code（授权码）对于第一次申请 FCC ID的客户。可在申请 FRN号后。申请 Grantee Code(需付费约60美金)，只需申请一次。FCC Grantee Code授权码注册链接：https://fjallfoss.fcc.gov/oetcf/eas/forms/GranteeRegistration.cfm&lt;br /&gt;
&lt;br /&gt;
*FCC ID包括Grantee Code 公司代号(3位或5位字母或数值)，每个Grantee Code只代表一间公司。该3位或5位号码由FCC随机提供，并非由客户自定。一旦申请成功,即成为固定的号码，作为该公司所有申请FCC ID 号码的前3位或5位代号。以及Product code产品的代号(1-14位字母或数值)。所以产品 ID号，前三位或者五位为 Grantee Code，后面由申请商自编(最多 14位)，通常用产品型号做自编码。&lt;br /&gt;
&lt;br /&gt;
*The label location information 。 FCC label 位置及其规格（铭牌），必须标明大小尺寸，以及在产品上的位置。 FCC label须包含 FCC ID号和 FCC警语，如果 label尺寸小，可只标明 FCC ID号，但 FCC警语一定要写在使用手册中（用户说明书）。其它如生产商，产品名称型号等信息可自行决定是否写在 label中。&lt;br /&gt;
&lt;br /&gt;
*Operational Description (Theory of Operation, Functional Description)。简单的工作原理，功能描述，请对产品的功能，用途，信号流程，各功能电路相互关系，电源供电做一个简短的说明。&lt;br /&gt;
&lt;br /&gt;
*Block Diagrams原理方框图，必须标明电路中所用到的任何晶振频率。&lt;br /&gt;
&lt;br /&gt;
*Circuit Schematics电路图，请确保清晰，其位号也需要看得清。&lt;br /&gt;
&lt;br /&gt;
*简单的使用说明User Manual，用户手册或使用说明书。&lt;br /&gt;
&lt;br /&gt;
*授权信&lt;br /&gt;
&lt;br /&gt;
*保密信(如需要保密)&lt;br /&gt;
&lt;br /&gt;
*提供申请FCC ID需要的样机，一般2台。&lt;br /&gt;
&lt;br /&gt;
 FCC ID证书官方查询网站：https://apps.fcc.gov/oetcf/eas/reports/GenericSearch.cfm&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E6%AC%A7%E6%B4%B2RED&amp;diff=154</id>
		<title>欧洲RED</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E6%AC%A7%E6%B4%B2RED&amp;diff=154"/>
		<updated>2019-07-05T15:38:58Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&#039;&#039;&#039;欧洲RED&#039;&#039;&#039;是指的是RED(Radio Equipment Directive) 电子电器产品的无线电指令，所有去欧洲的相关有意发射的RF电子电器产品都需要满足相关电磁兼容的标准，例如欧洲的电信联盟ETSI标准。&lt;br /&gt;
&lt;br /&gt;
 Directive 2014/53/EU of the European Parliament and of the Council of 16 April 2014 on the harmonisation of the laws of the Member States relating to the making available on the market of radio equipment and repealing Directive 1999/5/EC Text with EEA relevance. Applicable as of 13 June 2016.&lt;br /&gt;
 OJ L 153, 22.5.2014&lt;br /&gt;
&lt;br /&gt;
 为适应欧盟新立法框架（New Legislative Framework，NLF），2014年5月22日，欧盟官方期刊(L 153/62)公布了新版本的无线电设备指令2014/53/EU，用以替换原有的无线电及电信终端设备指令1999/5/EC。从2017年6月13号起RED 2014/53/EU指令正式代替RTTE 1999/5/EC指令。 2018年6月12日起，无线电设备投放市场前，制造商应针对低水平符合基本要求的无线电设备在中心系统进行设备类型注册登记。&lt;br /&gt;
&lt;br /&gt;
 RED指令的目的是：确保更为简便的市场准入以及对消费者健康和安全，以及家禽和财产更高水平的保护。为防止有害干扰，无线电设备应具有足够的电磁兼容水平并能有效使用无线电频谱和支持无线电频谱的有效利用。RED指令覆盖安全Safety、电磁兼容性EMC及无线电频谱RF要求。RED所涵盖的无线电设备不受低电压指令（LVD）或电磁兼容性指令（EMC）的约束：这些指令的基本要求由RED的基本要求所覆盖，但有一定的修改。&lt;br /&gt;
&lt;br /&gt;
 RED指令覆盖范围：工作频率在3000 GHz以下的所有无线电设备。包括短距离通讯设备，宽频带设备和移动通讯设备等，还覆盖仅用于声音接收和电视广播服务的无线电设备（例如，FM收音机和电视机）。例如：27.145 MHz无线遥控玩具，433.92 MHz 无线遥控器，2.4 GHz 蓝牙音箱，2.4 GHz/5 GHz WIFI空调和手机等任何内部具有RF有意发射频率的电子电器。&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;RED认证需要提供的资料&#039;&#039;&#039;&lt;br /&gt;
* 天线规格(或者天线增益图)&lt;br /&gt;
* 定频软件(也叫定频程式.使发射模块能够定在某一频率点持续发射,一般BT 和WIFI 一定要提供)&lt;br /&gt;
* Bill of Materials 元器件清单&lt;br /&gt;
* Block Diagram 原理框图&lt;br /&gt;
* Circuit Diagram 电路原理图&lt;br /&gt;
* Product Description and Concept of&lt;br /&gt;
* Operation 产品描述和工作原理描述&lt;br /&gt;
* Label Artwork标签丝印&lt;br /&gt;
* Marketing or Design 包装设计图&lt;br /&gt;
* PCB Layout 铜箔布线图&lt;br /&gt;
* Copy of Declaration of Conformity 符合性声明副本&lt;br /&gt;
* Sub‐Assemblies 装配图&lt;br /&gt;
* User Manual 用户手册&lt;br /&gt;
* Declaration on Model Difference 型号差异声明&lt;br /&gt;
* ISO 9001 Quality System Certification 质量体系证书&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=ESD&amp;diff=58</id>
		<title>ESD</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=ESD&amp;diff=58"/>
		<updated>2019-07-05T06:57:39Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&#039;&#039;&#039;ESD释义&#039;&#039;&#039;&lt;br /&gt;
* 全称是Electro-Static discharge，其中文意思是“静电放电”。是指具有不同静电荷电位的物体相互靠近或直接接触引起的电荷转移。简单说就是电荷瞬间从一个物体移到另一个物体上，形成一个电荷转移的过程的现象，即具有不同静电电势（电位差）的物体或表面之间的静电电荷转移，就是静电放电。在EMC领域我们习惯上称之为静电放电抗扰度试验，具体可参阅国际标准IEC-61000-4-2/GBT 17626.2，其中分接触放电和电磁场击穿介质放电。&lt;br /&gt;
&lt;br /&gt;
 静电释义：静电就是物体表面的一种处于相对稳定状态的电荷，它所产生的效应包括带电体之间力的作用和电场。&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;ESD实例&#039;&#039;&#039;&lt;br /&gt;
* 在雷雨天气产生的闪电，因为空气中有些尘埃粒子等所累积的正电与大地的负电相遇所产生放电的现象。&lt;br /&gt;
* 在干燥天气时，你触摸另一个人产生的电击感觉。&lt;br /&gt;
* 在铺有地毯的地板上行走后，手接触金属门把手产生的电击。&lt;br /&gt;
* 在冬天梳头发时，或者脱毛衣时产生的电火花现象。&lt;br /&gt;
&lt;br /&gt;
 ESD产生原理：具有不同静电荷电位的物体由于直接接触或静电感应所引起的物体之间静电电荷的转移。通常指在静电场的能量达到一定程度之后，击穿其间介质而进行放电的现象。&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;电荷的概念&#039;&#039;&#039;&lt;br /&gt;
* 电荷是物质、原子或电子等所带的电的量。单位是库仑（记号为C）。我们常将“带电粒子”称为电荷，但电荷本身并非“粒子”，只是我们常将它想像成粒子以方便描述。电荷只是量度而已，（世界上每样东西都带电荷，只是它本身由于带两种一正一负，且数量均等的电荷，才相互抵消。）&lt;br /&gt;
* 分子：保持物质化学性质的一种微粒；&lt;br /&gt;
* 原子：化学变化中的最小微粒，原子中心的原子核有质子和中子，环绕原子核运转的是电子；&lt;br /&gt;
* 电子：具有最小电量的质量最小的粒子(现在有分数电量之说)；&lt;br /&gt;
* 离子：以带正电(正离子)或负电(负离子)的原子或分子形态存在。&lt;br /&gt;
* 单晶体：按照一定规则的原子序列构成的晶体；&lt;br /&gt;
* 多晶体：小的单晶体的集合；&lt;br /&gt;
* 晶体：由反映晶体特征的基本单元在三维空间堆积而成的。把基本单元叫做晶胞；&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
* 质子数目＝电子数目     =〉电中性&lt;br /&gt;
* 质子数目&amp;gt;电子数目      =〉正电性&lt;br /&gt;
* 质子数目&amp;lt;电子数目      =〉负电性&lt;br /&gt;
* 同性电荷相斥，异性电荷相吸，并且导体上的电荷是可移动的，而绝缘体上的电荷是不可移动的，这就意味着绝缘体上的电荷是不能通过接地来中和的。&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;静电的产生&#039;&#039;&#039;&lt;br /&gt;
 静电产生的两种途径，静电是一种静止的电荷，是电子不均匀分布的结果，主要是摩擦产生，其他像电场诱发，直接充电等，即摩擦起电与感应起电。 &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;影响电荷量的因素&#039;&#039;&#039; &lt;br /&gt;
 摩擦电荷的极性与强度是由摩擦电序列决定，湿度愈高，静电愈低。55%湿度的静电产生量约为10%湿度的5-20%。其中还与电荷产生的速度；摩擦起电的相对位置；接触紧密程度；摩擦系数；分离速度.放电速度：材料的电导率；相对湿度；表面水汽分布；再接触的速度等甚至是还伴随一些不确定因素有关系。&lt;br /&gt;
&lt;br /&gt;
 &#039;&#039;&#039;摩擦起电&#039;&#039;&#039;&lt;br /&gt;
* 当两种不同性质的材料（至少其中一个为绝缘体)接触和分离，电荷从一种材料转移到另一种材料。&lt;br /&gt;
* 得到电荷的材料呈负电性，反之亦然。&lt;br /&gt;
* 产生电荷的类型与两种材料的相对位置有关。&lt;br /&gt;
任何两种材料摩擦后电极性都是可以判断的，在摩擦起电过程中，两者的距离越远，则各自产生的电荷越多。&lt;br /&gt;
&lt;br /&gt;
 &#039;&#039;&#039;感应起电&#039;&#039;&#039;&lt;br /&gt;
*非接触的方法&lt;br /&gt;
*当导电材料充分接近时,来源于某静电源的静电场将引起该导电材料表面的电荷分离。&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
 &#039;&#039;&#039;ESD静电放电模型&#039;&#039;&#039;&lt;br /&gt;
* &#039;&#039;&#039;HBM 人体放电模型(Human-Body Model, HBM)&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
人体模型（Human Body Model - HBM），HMB是ESD模型中建立最早和最主要的模型之一。&lt;br /&gt;
HBM是传统的测试模式，定义在工业标准 (MIL-STD-883x)中。人体上带电，特别在干燥的冬天，常会接触如门把手时便会有被电到的感觉。这是人体活动的结果，静电荷积聚在人体上，当我们去接触芯片时，人体上的静电就经由IC的pin脚进入芯片内部，然后经由IC放电到地。(不只在接触PIN时才会发生，因为封装IC的表面就存在静电荷，接触包装表面也会发生。)放电过程在瞬间发生，大概几纳秒内将IC组件烧毁。&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
* &#039;&#039;&#039;MM 机器放电模型 (Machine Model, MM)&#039;&#039;&#039;&lt;br /&gt;
&lt;br /&gt;
机器放电模式，也就是将人体换成了机器设备，主体部分的改变，使得测试模式的改变。在这情况下，指静电电荷积累在机器设备上，当接触到IC进对芯片放电，并因此毁坏了电路。机器放电模式，工业标准EIAJ-IC-121 method20。MM测试电路与HBM相似，数值改变如，电容值为200pf,充电电压500V,充电电阻100Mohms，放电部分加&amp;gt;500nH电感(电感量与电流无关，感抗XL=2πfL，f为频率)。因为绝大部分机器是金属的，等效电阻极小，导致瞬时放电电流巨大(几安培)。机器模型因在日本得到广泛应用，也叫日本模型。与家具模型不同的是它主要由200pf电容串非常低的电阻（&amp;lt;10Ω）代替通常串联的电阻构成。机器模型的典型代表如带电绝缘的机器人手臂、车辆、绝缘导体等。机器模型放电的波形与预料的家具模型波形相似，不同的是带电电容较大。典型的机器模型对小电阻（＜10Ω）放电的波形, 峰值电流可达几百安培，持续时间（决定于放电通路的电感）为几百纳。&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
* &#039;&#039;&#039;CDM 组件充电模式 (Charged-Device Model, CDM)&#039;&#039;&#039; &lt;br /&gt;
&lt;br /&gt;
这种模式下，电荷积聚在IC本身，可能是因为与PIN摩擦，或者是接触到其他物体的静电电荷，使本身带电。再通过直接接地或间接接地进行放电，而形成的一种放电现象。此类现象的模拟十分困难，是因为导致放电的组件差异所造成的。这种现象表明IC可能在生产过程中受损，比如IC在传输过程中带电，在安装到电路板上时接地而损坏。有时也可能在测试过程中受到损坏。CDM等效电路因情况的不同而多种多样。因为封装很小，所以电容和电感值都很小，大约5pf和10nH。CDM的放电时间很短，电流能在1ns时间内冲到15安培的高峰，因此这种现象更容易对IC造成损伤。CDM与HBM没有相互关连性，成功的CDM测试不能预示器件用HBM会发生什么情况!&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
* &#039;&#039;&#039;其它FIM/IEC/E-Gun 电磁场感应模式 (Field-Induced Model, FIM)&#039;&#039;&#039; &lt;br /&gt;
 &lt;br /&gt;
此类模式与CDM相似，只是IC带电方式不同。这种模式是IC在电场环境中，因感应而使本身带电，放电模式与CDM类拟。这种模式工业标准(JESD22-C101)，详情请阅读相关标准。&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=EMI&amp;diff=54</id>
		<title>EMI</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=EMI&amp;diff=54"/>
		<updated>2019-07-05T06:41:03Z</updated>

		<summary type="html">&lt;p&gt;EMC：​&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&#039;&#039;&#039;EMI(Electro Magnetic Interference)&#039;&#039;&#039;：直译是电磁干扰，是指它对外界发射的电磁骚扰。这是合成词，我们应该分别考虑&amp;quot;电磁&amp;quot;和&amp;quot;干扰&amp;quot;。 所谓&amp;quot;干扰&amp;quot;，指设备受到干扰后性能降低以及对设备产生干扰的干扰源这二层意思。第一层意思如雷电使收音机产生杂音，摩托车在附近行驶后电视画面出现雪花，拿起电话后听到无线电声音等。&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;电磁干扰（EMI）测试&#039;&#039;&#039;&lt;br /&gt;
* 空间辐射测试（RE）传导辐射测试（CE）&lt;br /&gt;
* 骚扰功率测试（Disturbance Power Test）&lt;br /&gt;
* 电源谐波测试（Harmonics Test）&lt;br /&gt;
* 电压闪烁测试（Flicker Test）&lt;br /&gt;
* 不连续干扰测试（Click Test）&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E6%AC%A7%E6%B4%B2BT%E8%93%9D%E7%89%99%E8%AE%A4%E8%AF%81&amp;diff=148</id>
		<title>欧洲BT蓝牙认证</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E6%AC%A7%E6%B4%B2BT%E8%93%9D%E7%89%99%E8%AE%A4%E8%AF%81&amp;diff=148"/>
		<updated>2019-07-04T03:26:03Z</updated>

		<summary type="html">&lt;p&gt;EMC：​BT蓝牙认证&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;蓝牙无线产品，做欧洲无线RED认证，需要做哪些标准？&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;RED射频RF标准&#039;&#039;&#039;&lt;br /&gt;
 EN 300328 V2.1.1&lt;br /&gt;
 EN 301489-1 V2.1.1&lt;br /&gt;
 EN 301489-17 V3.1.1&lt;br /&gt;
 EN 62479&lt;br /&gt;
&lt;br /&gt;
无意发射EMC部分，依据不同的产品，采用不同的产品标准，如下以蓝牙音箱为例子&lt;br /&gt;
&#039;&#039;&#039;EMC标准&#039;&#039;&#039;&lt;br /&gt;
 EN 61000-3-2&lt;br /&gt;
 EN 61000-3-3&lt;br /&gt;
 EN 55032&lt;br /&gt;
 EN 55024 or EN 55035&lt;br /&gt;
 &lt;br /&gt;
如果嵌入在某类型产品里面，则需要满足相对应的产品标准，例如多媒体产品则需要满足：&lt;br /&gt;
&#039;&#039;&#039;低电压指令LVD&#039;&#039;&#039;&lt;br /&gt;
 EN62368 or EN 60950&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=%E8%93%9D%E7%89%99RED%E8%AE%A4%E8%AF%81&amp;diff=176</id>
		<title>蓝牙RED认证</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=%E8%93%9D%E7%89%99RED%E8%AE%A4%E8%AF%81&amp;diff=176"/>
		<updated>2019-07-03T09:13:25Z</updated>

		<summary type="html">&lt;p&gt;EMC：​蓝牙无线产品做欧洲RED认证，需要做哪些标准&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;蓝牙无线产品，做欧洲无线RED认证，需要做哪些标准？&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;有意发射RF射频部分&#039;&#039;&#039;&lt;br /&gt;
* EN 300328 V2.1.1&lt;br /&gt;
* EN 301489-1 V2.1.1&lt;br /&gt;
* EN 301489-17 V3.1.1&lt;br /&gt;
* EN 62479&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;无意发射EMC部分，依据不同的产品，采用不同的产品标准，如下以蓝牙音箱为例子&#039;&#039;&#039;&lt;br /&gt;
* EN 61000-3-2&lt;br /&gt;
* EN 61000-3-3&lt;br /&gt;
* EN 55032&lt;br /&gt;
* EN 55024&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;低电压指令LVD&#039;&#039;&#039;&lt;br /&gt;
* EN62368 or EN 60950&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
	<entry>
		<id>https://www.iec.wiki/index.php?title=CE%E8%AE%A4%E8%AF%81&amp;diff=30</id>
		<title>CE认证</title>
		<link rel="alternate" type="text/html" href="https://www.iec.wiki/index.php?title=CE%E8%AE%A4%E8%AF%81&amp;diff=30"/>
		<updated>2019-06-23T13:44:45Z</updated>

		<summary type="html">&lt;p&gt;EMC：​CE认证&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;在欧盟市场“CE”标志属强制性认证标志，不论是欧盟内部企业生产的产品，还是其他国家生产的产品，要想在欧盟市场上自由流通，就必须加贴“CE”标志，以表明产品符合欧盟《技术协调与标准化新方法》指令的基本要求。&lt;br /&gt;
&lt;br /&gt;
词意起源&lt;br /&gt;
CE是法语的缩写，英文意思为 “European Conformity 即欧洲共同体，原来用英语词组EUROPEAN COMMUNITY 缩写为EC，后因欧共体在法文是COMMUNATE EUROPEIA，意大利文为COMUNITA EUROPEA，葡萄牙文为 COMUNIDADE EUROPEIA，西班牙文为COMUNIDADE EUROPE等，故改EC为CE。当然，也不妨把CE视为CONFORMITY WITH EUROPEAN （DEMAND）（符合欧洲（要求）），CE 标志是安全合格标志而非质量合格标志。&lt;br /&gt;
&lt;br /&gt;
发证机构&lt;br /&gt;
 （1）企业自主签发的Declaration of conformity / Declaration of compliance《符合性声明书》，此证书属于自我声明书，不应由第三方机构（中介或测试认证机构）签发，因此，可以用欧盟格式的企业《符合性声明书》代替。&lt;br /&gt;
 （2）Certificate of compliance / Certificate of compliance《符合性证书》，此为第三方机构（中介或测试认证机构）颁发的符合性声明，必须附有测试报告等技术资料TCF，同时，企业也要签署《符合性声明书》。&lt;br /&gt;
 （3）EC Attestation of conformity 《欧盟标准符合性证明书》，此为欧盟公告机构（Notified Body简写为NB）颁发的证书，按照欧盟法规，只有NB才有资格颁发EC Type的CE声明。&lt;br /&gt;
&lt;br /&gt;
CE包含&lt;br /&gt;
 1，LVD：低电压指令 Low Voltage Directive，指令适用范围是使用电压为交流在50V至1000V和直流75V至1500V之间的电器产品。LVD 的目标为确保低电压设备在使用时的安全性。&lt;br /&gt;
 2，EMC：电磁兼容性Electro Magnetic Compatibility，是指设备或系统在其电磁环境中符合要求运行并不对其环境中的任何设备产生无法忍受的电磁干扰的能力。&lt;br /&gt;
      EMC包括两个方面的要求：&lt;br /&gt;
     （1）是指设备在正常运行过程中对所在环境产生的电磁干扰不能超过一定的限值，称为EMI。&lt;br /&gt;
     （2）面是指器具对所在环境中存在的电磁干扰具有一定程度的抗扰度，即电磁敏感性，称为EMS。&lt;br /&gt;
&lt;br /&gt;
3，RoHS：Restriction of Hazardous Substances, 全称是《关于限制在电子电器设备中使用某些有害成分的指令》, 由欧盟立法制定的一项强制性标准。&lt;br /&gt;
&lt;br /&gt;
4，ErP：能源相关产品 Energy-related Products, 对产品设置了最低性能和能耗要求，而且要求生产商和进口商去评估产品整个生命周期的环境影响要素并且基于该评估结果来优化设计方案，以达到改善产品的环境影响的目的。&lt;br /&gt;
&lt;br /&gt;
5，RED，针对无线通讯产品的CE指令， Radio Equipment Directive，即无线电设备指令。&lt;br /&gt;
……&lt;/div&gt;</summary>
		<author><name>EMC</name></author>
	</entry>
</feed>