EMC China Lab

Introduction to CB Certification for Lighting

Views :
Update time : 2024-06-30

The IECEE-CB scheme is a global mutual recognition system for the safety testing resULts of electrical products. Through a single test, manufacturers can obtain a cb test certificate and report, which can then be used to apply for certifications in multiple countries within the CB scheme without the need for repeated testing. When applying, it is essential to specify the countries to be included in the report so that their specific requirements can be coveRED during the testing.

 

Introduction to CB Certification for Lighting(图1)


Lighting cb certification Testing Standards

- General requirements for lighting: iec 60598-1

- Fixed general-purpose luminaires: IEC 60598-2-1

- Recessed luminaires: IEC 60598-2-2

- Road and street lighting: IEC 60598-2-3

- Portable general-purpose luminaires: IEC 60598-2-4

- Floodlights: IEC 60598-2-5

- Hand lamps: IEC 60598-2-8

- Portable general-purpose luminaires for children: IEC 60598-2-10

- Aquarium lighting: IEC 60598-2-11

- Nightlights with built-in power sockets: IEC 60598-2-12

- Ground recessed luminaires: IEC 60598-2-13

- Stage lighting: IEC 60598-2-17

- String lights: IEC 60598-2-20

- Sealed string lights: IEC 60598-2-21

- Emergency lighting luminaires: IEC 60598-2-22

 

Required Documentation for Lighting CB Certification

1. Application form, trademark declaration letter, declaration of conformity

2. Product manual

3. Product specification

4. Circuit diagram

5. PCB layout

6. Specifications of key components

7. CDF key components list

8. BOM list

9. CB label, etc.

 

Important Considerations for Applying for a cb certificate for Lighting

1. When applying for CB certification, it is necessary to inform which countries are to be included in the report so that the corresponding national differences can be taken into account during testing.

2. When applying for CB certification, if subsequent IECEE registration is required, be sure to confirm the information of the applicant and the manufacturer (the IECEE registration certificate will only reflect the information of the manufacturer/importer).

3. For each signed document in the CB to IECEE registration process, be sure to use company letterhead.

 

China JJR Laboratory is an IEC 17025 authorized laboratory, providing CB certification services for lighting. We are located in China and can help you save 30% on certification costs.


Email:hello@jjrlab.com


Leave Your Message


Write your message here and send it to us


Related News
Read More >>
USA FDA Food Contact Material (FCM) Test Report USA FDA Food Contact Material (FCM) Test Report
01 .12.2026
FDA FCM testing ensures food-contact materials meet safety standards (CFR 21). JJR Lab provides ISO ...
FCM Food Contact Materials Certification FCM Food Contact Materials Certification
01 .12.2026
TEMU FCM Materials Testing by JJR Lab: EC1935/2004, covering migration, heavy metals, sensory & ...
SCC-Accredited CSA C22.2 No.42 Test Report Amazon SCC-Accredited CSA C22.2 No.42 Test Report Amazon
01 .12.2026
Amazon Canada requires CSA C22.2 No.42 USB test reports from SCC-accredited labs like JJR Lab to ens...
Compliance Tips for Button & Coin Cell Batteri Compliance Tips for Button & Coin Cell Batteri
01 .12.2026
Amazon US requires button/coin batteries to meet Reese Law child-resistant packaging and warning lab...
16 CFR 1243 & Nursing Pillow 16 CFR 1242/ASTM 16 CFR 1243 & Nursing Pillow 16 CFR 1242/ASTM
01 .12.2026
Amazon infant support & nursing pillows must meet 16 CFR 1243/1242 & ASTM F3669-24. JJR Lab ...
Two Approaches to Amazon Toy TIC Audit Two Approaches to Amazon Toy TIC Audit
01 .12.2026
Amazon enforces Toy TIC Direct Validation via two methods: TIC testing or lab verification by approv...
TIC Direct Validation for Power Banks and Lithium TIC Direct Validation for Power Banks and Lithium
01 .12.2026
Amazon mandates TIC Direct Validation for power banks; sellers must pass UL2056, IEC62368-1, UN38.3 ...
European Authorized Representative for Medical Dev European Authorized Representative for Medical Dev
01 .11.2026
JJR provides EU Authorized Representative service for medical devices, ensuring MDR compliance, ISO ...

Leave Your Message