EMC China Lab

What is the UL 60950 Test Report?

Views :
Update time : 2025-02-20

UL 60950 is a North American safety standard for IT power supplies. It is a safety regulation that primarily focuses on product safety aspects such as temperature rise, dielectric strength, insulation, etc. Different products and regions have different safety standards.

 

For example, IT power supplies follow the UL 60950 standard, while audiovisual power supplies adhere to the UL 60065 standard. There are, of course, many other safety standards as well.

 

What is the UL 60950 Test Report?(图1)


UL 60950 Test Items:

1. Output voltage, current, and V-A testing 

2. Double or reinforced insulation testing for bridging components 

3. Input testing 

4. Safety Extra Low Voltage (SELV) stability testing 

5. Power-limited power supply testing 

6. Transformer/insulation depth testing 

7. Humidity testing 

8. Operating voltage testing 

9. Hazardous voltage circuit testing 

10. Stress relief testing 

11. Stability dielectric strength testing 

12. Drop test 

13. Torque testing for plug-in devices 

14. Constant force testing for plug-in device blades 

15. Contact safety testing for plug-in device inputs 

16. Touch current testing for single-phase equipment 

17. Thermal testing 

18. Ball pressure test 

19. Dielectric strength test 

20. Component failure testing 

21. Abnormal transformer testing 

22. Power output short-circuit/overload testing 

 

UL 60950 Processing Time & Cost

The processing time for UL 60950 certification is typically **5-7 working days**, with costs determined based on the specific product.


Email:hello@jjrlab.com


Leave Your Message


Write your message here and send it to us


Related News
Read More >>
Biological Evaluation of Medical Devices ISO 10993 Biological Evaluation of Medical Devices ISO 10993
04 .16.2026
JJR LAB performs ISO 10993 biological evaluations to ensure medical devices are safe for human use, ...
In Vitro Cytotoxicity Test for Biomedical Devices In Vitro Cytotoxicity Test for Biomedical Devices
04 .16.2026
JJR LAB conducts ISO 10993-5 in vitro cytotoxicity tests to ensure medical device safety, assessing ...
EU Responsible Person on Amazon EU Responsible Person on Amazon
04 .16.2026
EU Responsible Person is EU rep for non-EEA manufacturers ensuring compliance and regulatory require...
GPSR EU Responsible Person Service GPSR EU Responsible Person Service
04 .16.2026
EU Responsible Person compliance is essential for selling in Europe, covering requirements, risks, a...
UK Responsible Person for Medical Devices UK Responsible Person for Medical Devices
04 .16.2026
UK rules clarify UK Responsible Person info: required for UKCA, not CE, but always MHRA-registered. ...
UK Cosmetics Responsible Person Service UK Cosmetics Responsible Person Service
04 .16.2026
JJR LAB’s UK Cosmetics Responsible Person Service ensures imported products meet UK labeling rules, ...
FDA Registration US Agent FDA Registration US Agent
04 .15.2026
FDA registration requires foreign mfrs to appoint a US Agent to liaise with FDA, handle inspections,...
ASTM F963 Toy Safety Standard ASTM F963 Toy Safety Standard
04 .15.2026
ASTM F963 defines mandatory toy safety rules covering mechanical chemical electrical flammability an...

Leave Your Message