Sorry for the abrupt response but time is short and there are I believe
there are serious issues here.
If you would like to take some of these points off line please email me.
A Class III LASER is dangerous!
For UL/CSA you will need a FDA report. I have just completed just such a
project.
For CE Marking you might use that report (some may disagree because if it
not of the EU).
If you even need a CB Report you will need a IEC 825 (Number??) LASER REPORT
An OPEN ??? are there interlocks? - processes? - operating instruction?
The unit is definitely NOT a COMPONENT Nor can it ever be considered as
such.
Even if it was a component you WOULD NOT be able to sent it round the world.
There are many differing requirements - I'll leave it to people better
qualified (like John Woodgate) to give you the details (please John).
P.O. Box 310, Reedville,
Virginia 22539 USA
Phone: (804) 453-3141
Fax: (804) 453-9039
Web: www.test4safety.com
free eLearning Solutions
If the product only was a component I would just send it around the
world but it can function as a product by just adding a PC to a RS 232
port.
How should I tread this product when sending it to US/Canada ?
Can I just add a label on the product with a text like this:
For evaluation purpose only ?
And what about EU, the manufacturer is located in EU ?
Best regards,
Kim Boll Jensen
Bolls Raadgivning
Consultant in type approvals
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