UKCA英國符合性評估對市場的影響是什么呢？
目前，UKCA認證體系與CE認證體系非常相似，因此在幾乎所有情況下，凡是要求進入歐盟市場前加貼CE標志的，也同樣要求進入英國市場前加貼UKCA標志。該標志主要加貼在產(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
標志和標簽
如果從歐盟進口，我需要在產(chǎn)品上注明英國地址嗎？
是的，進口商地址也應(yīng)在產(chǎn)品上注明。對于在產(chǎn)品上注明進口商詳細資料不可行的情況，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。