包拿证,亚科检测是专业做CE认证机构,与欧盟公告机构和各国家单位紧密合作,关于费用价格多少钱,时间多少天多久,需要提供哪些资料流程,欢迎随时咨询。
CE认证即只限于产品不危及人类、动物和货品的安全方面的基本安全要求,而不是一般质量要求,协调指令只规定主要要求,一般指令要求是标准的任务。因此准确的含义是:CE标志是安全合格标志而非质量合格标志。是构成欧洲指令核心的"主要要求"。
CE认证适用企业:制造商、贸易商、进口商、分销商等一系列涉及企业。
CE认证适用产品:一般凡是出口到欧盟国家的产品都要满足CE认证标准,如:电子电器类、机械产品、电梯、建材、日用品等。
The
NewLegislative Framework consists of:
Regulation
(EC)765/2008 setting out the requirements for accreditation and themarket
surveillance of products;
Decision768/2008
on a common framework for the marketing of products,which includes reference
provisions to be incorporated whenever productlegislation is revised. In
effect, it is a template for future productharmonisation legislation;
Regulation
(EC)764/2008 laying down procedures relating to the application ofcertain
national technical rules to products lawfully marketed in another EUcountry.
Alignment
of product legislation;
A
main objective of the Commission is tobring product harmonisation legislation
in line with the reference provisionsof Decision768/2008/EC. The following
directives and regulations were alignedwith these reference provisions:
Low
Voltage -Directive 2014/35/EU
ElectromagneticCompatibility
- Directive 2014/30/EU
Machinery
(MD) 2006/42/EC
Toy
Safety -Directive 2009/48/EU
Transportablepressure
equipment - Directive 2010/35/EU
Restriction
ofHazardous Substances in Electrical and Electronic Equipment -
Directive2011/65/EU
Constructionproducts
- Regulation (EU) No 305/2011
PyrotechnicArticles
- Directive 2013/29/EU
Recreationalcraft
and personal watercraft - Directive 2013/53/EU
Civil
Explosives- Directive 2014/28/EU
Simple
PressureVessels - Directive 2014/29/EU
Non-automaticWeighing
Instruments - Directive 2014/31/EU
MeasuringInstruments
- Directive 2014/32/EU
Lifts
-Directive 2014/33/EU 金华光伏连接器CE认证EN50521检测
ATEX
- Directive2014/34/EU
Radio
equipment- Directive 2014/53/EU
Pressureequipment
- Directive 2014/68/EU
Marine
Equipment- Directive 2014/90/EU
Cablewayinstallations
- Regulation (EU) 2016/424
Personalprotective
equipment - Regulation (EU) 2016/425
Gas
appliances -Regulation (EU) 2016/426
Medical
devices- Regulation (EU) 2017/745
In
vitro diagnosticmedical devices - Regulation (EU) 2017/746
亚科检测成功案例非常多。拥有深耕认证行业多年的认证工程师,经验丰富,可以专业地为企业提供检测整改认证一站式服务。