欧盟CE
一、什么是CE?
CE 标志为欧盟强制性验证标志,被视为制造商打开并进入欧洲市场的护照。凡是贴有 “CE” 标志的产品就可在欧盟各成员国内销售,无须符合每个成员国的要求,从而实现了商品在欧盟成员国范围内的自由流通。市场上销售的商品如被欧盟 New Approach 指令所要求需符合 CE 验证,产品本身则需符合欧盟相关指令的验证并在产品本身及使用说明上加贴 CE 标志,加贴 CE 验证标志的商品表示其符合欧盟指令规范。
二、规范内容:参考欧盟标准
European-Standards | ||
1 | Machinery Directive | 2006/42/EC |
2 | Low Voltage Directive | 2014/35/EU |
3 | EMC Directive | 2014/30/EU |
4 | Medical Devices Directive | 2017/745 |
5 | Personal Protective Equipment Directive | 2016/425 |
6 | Construction Products (CPD/CPR) | 93/68/EEC |
7 | Pressure Equipment Directive | 2014/68/EU |
8 | RoHS | 2011/65/EU |
9 | Waste Electrical and Electronic Equipment Directive | 2012/19/EU |
10 | ATEX Directive | 2014/34/EU |
11 | Toy safety | 2009/48/EC |
12 | Radio Equipment Directive | 2014/53/EU |
13 | Recreational Craft Directive | 94/25/EC |
14 | Active Implantable Medical Devices Directive | 2017/745 |
15 | Explosive for Civil Use Directive | 2014/28/EU |
16 | Noise Emission in the Environment Directive | 2016/426 |
17 | Gas Appliances Directive | 2016/426/EU |
18 | Lifts Directive | 2014/33/EU |
19 | Pyrotechnic Directive | 2013/29/EU |
20 | Measuring instruments (MID) | 2014/32/EU |
21 | Chemical substances (REACH) | No.1907/2006 |
22 | Fertilising products | No.2019/1009 |
23 | Cosmetics products | No 1223/2009 |
24 | General product safety | 2023/988 |
25 | In vitro diagnostic medical devices (Regulation 2017/746) | 2017/746 |
26 | Non-automatic weighing instruments (NAWI) | 2014/31/EU |
27 | Cableway installations | 2016/424 |
28 | Inspection of pesticide application equipment | 2009/128/EC |
29 | Rail system | 2016/797 |
30 | Simple Pressure Vessels (SPVD) | 2014/29/EU |
31 | Unmanned aircraft systems (UAS) | 2019/945 |
32 | Community postal services | 97/67/EC |
33 | Packaging and packaging waste | 2005/20/EC |
34 | Plastic caps and lids | 2019/904 |
三、适用产品:
四、验证申请流程: