Charlie:

 

Yes, there is a cost effective alternate option for Class 1 laser
certification.

 

FDA does not object testing to IEC 60825-1 (Laser Notice No.50) instead of 21
CFR 1040.10 (ANSI Z136.1) http://www.fd
.gov/MedicalDevices/DeviceRegulationand
uidance/GuidanceDocuments/ucm094361.htm  

 

For USA market, laser product should be tested by recognized NRTL to
applicable OSHA standards, not to UL requirements.

 

Don’t argue with UL.

 

Use another NRTL:  http://www.osha.gov/dts/otpca/nrtl/nrtllist.html

 

Submit to TUV Product Service for testing to UL/CSA 60950-1, EN 60950-1 and EN
60825-1 (IEC 60825-1) for one genuine TUV CUE mark recognized for USA (NRTL),
Canada (CSA) and EU:

http://www.tuvamerica.com/services/electrical/cue.cfm

 

Best regards,

 

Samuel

 

 

________________________________

From: emc-p...@ieee.org [mailto:emc-p...@ieee.org] On Behalf Of Charlie
Blackham
Sent: Thursday, April 01, 2010 8:07 AM
To: 'EMC-PSTC'
Subject: UL60950-1 requirements for lasers

 

Group

 

Have a piece of UL60950-1 telecoms equipment containing a laser:

 

The laser has 3rd party report to IEC60825 

 

Given the accepted similarities between 21CFR1040 and IEC60825 as detailed in
FDA Laser Notice 50 - has anyone successfully used “an IEC60825 report and
laser Notice no.50” to meet this requirement for UL?

 

(UL are currently insisting on a full CDRH report.)

 

Regards

Charlie

 

 

 

 

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