Hopefully, your spam filters didn’t filter out w-e-e-e.

 

Anyway,  one of our managers brought up a good point.

 

He was wondering what kind of “proof” would manufacturers offer for CE
marking to these directives???

 

It seems to me that this is a truly self-declaration type of standard, whereby
the manufacturer (us, for instance) must keep documentation and spec sheets
showing that component parts meet the directive.

 

I can’t imagine a “test” that could be done by a third party lab…other
than taking a product, throwing it through a stump grinder and then analyzing
the chips for Lead residue.  (Although I could do that test for a small fee
:-))

 

Would a few of you be willing to share how you are planning to stack up their
“evidence” to show compliance to this directive?  Are you just going to
keep component part specs? Have independent laboratory testing performed? 
Both?

 

Thanks,

 

Chris Maxwell

Design Engineer

Nettest

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