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UKCA英國符合性評估對市場的影響是什么呢？

目前，UKCA認(rèn)證體系與CE認(rèn)證體系非常相似，因此在幾乎所有情況下，凡是要求進(jìn)入歐盟市場前加貼CE標(biāo)志的，也同樣要求進(jìn)入英國市場前加貼UKCA標(biāo)志。該標(biāo)志主要加貼在產(chǎn)品上，通常也加貼在包裝上（在少數(shù)情況下也接受標(biāo)示于隨附文件上）。具體將在適用于您的產(chǎn)品的法規(guī)中加以定義。

歐盟與英國市場要求對比

歐盟法規(guī)	英國法規(guī)
ATEX - Directive 2014/34/EU	Equipment and Protective Systems Intended for use in Potentially Explosive Atmospheres Regulations 2016
Electromagnetic Compatibility - Directive 2014/30/EU	Electromagnetic Compatibility Regulations 2016
Lifts - Directive 2014/33/EU	Lifts Regulations 2016
Low Voltage - Directive 2014/35	Electrical Equipment (Safety) Regulations 2016
Machinery - Directive 2006/42/EC	Supply of Machinery (Safety) Regulations 2008
Outdoor Noise - Directive 2000/14/EC	Noise Emission in the Environment by Equipment for use Outdoors Regulations 2001
Personal Protective Equipment Regulation - 2016/425 (PPE)	Regulation 2016/425 on Personal Protective Equipment as brought into UK law and amended
Pressure Equipment - Directive 2014/68/EU	Pressure Equipment (Safety) Regulations 2016
Radio Equipment - Directive 2014/53/EU	Radio Equipment Regulations 2017
Simple Pressure Vessels - Directive 2014/29/EU	Simple Pressure Vessels (Safety) Regulations 2016
Toy Safety - Directive 2009/48/EC	Toys (Safety) Regulations 2011

歐盟法規(guī)

英國法規(guī)(英國皇家認(rèn)可委員會和英國藥品和健康產(chǎn)品管理局)

Medical Devices Regulation - 2017/745 (MDR)

In Vitro Diagnostics Regulation - 2017/746 (IVDR)

Medical Devices Regulations 2002

(The following EU Directives are given effect in UK law through the MDR 2002: Directive 93/42/EEC (medical devices), Directive 90/385/EEC (active implantable), and Directive 98/79/EC (in vitro diagnostics))

常見問題——英國法規(guī)的影響

標(biāo)志和標(biāo)簽

如果從歐盟進(jìn)口，我需要在產(chǎn)品上注明英國地址嗎？

是的，進(jìn)口商地址也應(yīng)在產(chǎn)品上注明。對于在產(chǎn)品上注明進(jìn)口商詳細(xì)資料不可行的情況，針對貴方產(chǎn)品的法規(guī)可能會將其考慮在內(nèi)，允許在它處注明。

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UKCA英國符合性評估對市場的影響