EMC China Lab

Which Country Issues CE Certification?

Views :
Update time : 2024-06-17

Applicable Countries for CE certification

CE certification is applicable in 32 econoMIC areas in Europe, including the 28 EU member states, 3 out of 4 EFTA countries, and Turkey. Products with the CE mark can be freely circULated within the European Economic Area (EEA). The specific list of the 28 EU countries is as follows: Belgium, Bulgaria, Czech Republic, Denmark, Germany, Estonia, Ireland, Greece, Spain, France, Croatia, Italy, Cyprus, Latvia, Lithuania, Luxembourg, Hungary, Malta, Netherlands, Austria, Poland, Portugal, Romania, Slovenia, Slovakia, Finland, Sweden, and the United Kingdom.

 

Which Countries Require CE Certification?

1. EFTA (European Free Trade Association) includes four member countries (Iceland, Norway, Switzerland, and Liechtenstein), but the CE mark is not mandatory within Switzerland.

2. Due to the colonial era, CE certification is widely recognized globally. Some countries in Africa, Southeast Asia, and Central Asia may also accept CE certification.

3. As of November 2019, the Brexit process is ongoing, and subsequent results are pending.

 

Product Range CoveRED by CE Certification

To understand the product range of CE certification, one must be familiar with the NLF regulations. The NLF (New Legislative Framework) specifies which products require CE certification. The EU's NLF currently includes 22 directives, which are:

 

1. Toy Safety - Directive 2009/48/EC

2. Transportable Pressure Equipment - Directive 2010/35/EU

3. Restriction of Hazardous Substances in Electrical and Electronic Equipment - Directive 2011/65/EU

4. Construction Products - Regulation (EU) No 305/2011

5. Pyrotechnic Articles - Directive 2013/29/EU

6. Recreational Craft and Personal Watercraft - Directive 2013/53/EU

7. Civil Explosives - Directive 2014/28/EU

8. Simple Pressure Vessels - Directive 2014/29/EU

9. Electromagnetic Compatibility - Directive 2014/30/EU

10. Non-Automatic Weighing Instruments - Directive 2014/31/EU

11. Measuring Instruments - Directive 2014/32/EU

12. Lifts - Directive 2014/33/EU

13. Equipment and Protective Systems Intended for Use in Potentially Explosive Atmospheres (ATEX) - Directive 2014/34/EU

14. Radio Equipment - Directive 2014/53/EU

15. Low Voltage - Directive 2014/35/EU

16. Pressure Equipment - Directive 2014/68/EU

17. Marine Equipment - Directive 2014/90/EU

18. Cableway Installations - Regulation (EU) 2016/424

19. Personal Protective Equipment - Regulation (EU) 2016/425

20. Gas Appliances - Regulation (EU) 2016/426

21. Medical Devices - Regulation (EU) 2017/745

22. In Vitro Diagnostic Medical Devices - Regulation (EU) 2017/746

 

Notes

NLF refers to the New Legislative Framework of the EU, which was adopted in 2008 to strengthen the market surveillance framework and recognition system for products. It provides unified definitions for concepts in the original New Approach Directives, sets out specific provisions for national accreditation bodies and systems, EC market surveillance frameworks, product market access control, the use of marks, and EC funding.

 

If you need to obtain CE certification, please contact us for consultation.


Email:hello@jjrlab.com


Leave Your Message


Write your message here and send it to us


Related News
Read More >>
Infant Support Pillow 16 CFR 1243/1242 & ASTM Infant Support Pillow 16 CFR 1243/1242 & ASTM
12 .19.2025
Infant Support & Nursing Pillows must meet CPSC 2025 rules, including 16 CFR 1243/1242 & AST...
BRM Registration Card Under CFR Part 1130 Regulati BRM Registration Card Under CFR Part 1130 Regulati
12 .19.2025
Required for CFR Part 1130 infant products, the BRM Card supports CPC compliance and U.S. address ve...
How to get a D-U-N-S® Number for US FDA Registrati How to get a D-U-N-S® Number for US FDA Registrati
12 .18.2025
Get your D-U-N-S® Number for FDA registration. JJR LAB helps medical device firms apply fast, meet t...
Household Massage Devices Compliance in the China Household Massage Devices Compliance in the China
12 .18.2025
JJR LAB ensures household massage devices comply in China & Japan: CQC (GB4706.1/10), PSE (J/IEC...
Compliance for the Global In Vitro Diagnostic (IVD Compliance for the Global In Vitro Diagnostic (IVD
12 .18.2025
JJR LAB, ISO/IEC 17025 certified, offers one-stop IVD device compliance testing & certification ...
Compliance Guide for Nebulizers in European and Am Compliance Guide for Nebulizers in European and Am
12 .18.2025
JJR LAB provides CE/FDA nebulizer testing (IEC 60601, ISO 27427, ISO 18562, ISO 10993) covering perf...
Cybersecurity Certification Service for EU RED Dir Cybersecurity Certification Service for EU RED Dir
12 .18.2025
JJR Lab provides RED 3.3(d/e/f) compliance via EN18031-1/2/3 testing, offering asset review, securit...
ANATEL Certification Compliance Guide for Brazil M ANATEL Certification Compliance Guide for Brazil M
12 .18.2025
ANATEL compliance ensures RF/EMC/safety testing to Brazil standards; required for wireless/network d...

Leave Your Message