The EN 60825 'process' is simple. This is a 'self-declaration' route. There
is no 
authority that I am aware of at this time (like the CDRH in the US) to which
the documentation needs to be submitted.

It's as basic performing the required tests as prescribed in the standard
and
creating a report. Of course there a variety of documentation on the product
which 
should be assembled. 

Of course this is an over-simplification, because the some of the testing
(fault generation in particular) can get tedious, and the time/complexity
involved is proportional to the
complexity/features of the circuitry of the product.

Sound engineering judgement will also need to be made in the ultimate
classification of the
product taking into consideration the use of the end product by what type of
individual, and
the installation location with regards to accessibility of the product. The
classification is not only dependent upon wavelength, power, beam
divergence, etc . . . 

Hope this helps. If you need more detail, feel free to contact me off-line.

John A. Juhasz
Product Qualification &
Compliance Engr.

Fiber Options, Inc.
80 Orville Dr. Suite 102
Bohemia, NY 11716 USA

Tel: 631-419-2324
Fax: 631-567-8322 



-----Original Message-----
From: Lubeski, Paul [mailto:[email protected]]
Sent: Tuesday, March 07, 2000 4:53 PM
To: IEEE ORG
Cc: Loop, Robert
Subject: EN60825



All:

We are looking for information on what the process is for getting a Class II
laser device approval to EN60825 in Europe.

Thanks in advance for any information that can be provided.


Paul A. Lubeski
Senior Engineer
Wyle Laboratories, Inc.
7800 HWY 20 W.
Huntsville, AL  35806
(256) 837-4411 ext. 494
(256) 830-0904 fax
[email protected]

http://www.wylelabs.com 


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