UKCA英国符合性评估对市场的影响是什么呢？
目前，UKCA认证体系与CE认证体系非常相似，因此在几乎所有情况下，凡是要求进入欧盟市场前加贴CE标志的，也同样要求进入英国市场前加贴UKCA标志。该标志主要加贴在产品上，通常也加贴在包装上（在少数情况下也接受标示于随附文件上）。具体将在适用于您的产品的法规中加以定义。
欧盟与英国市场要求对比
欧盟法规 | 英国法规 |
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 |
欧盟法规 | 英国法规(英国皇家认可委员会和英国药品和健康产品管理局) |
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)) |
常见问题——英国法规的影响
标志和标签
如果从欧盟进口，我需要在产品上注明英国地址吗？
是的，进口商地址也应在产品上注明。对于在产品上注明进口商详细资料不可行的情况，针对贵方产品的法规可能会将其考虑在内，允许在它处注明。