Hi Gary,

Your only requirement is ROHS. If your customers need evidence or question EMC 
and Product Safety, you can then justify your steps taken to attain Due 
Diligence to the specific applicable standards.

Regards,
Mark

From: McInturff, Gary [mailto:[email protected]]
Sent: Friday, December 09, 2011 2:01 PM
To: [email protected]
Subject: [PSES] DoC - maybe asked and answered but looking for one more answer

Knowing there are directives for EMC, Safety, and RoHS compliance I am a bit 
uncertain what to do with a subassembly which is in itself incomplete and not 
fully functional but requires entry into the EU so that it can become part of a 
larger system - also requiring all the regulations.

We build and generate DoC's and apply the CE mark as appropriate for end units 
and reference the EU directives that apply. I seem to have two choices on the 
subassemblies
Acknowledge that the end product will have all of the directives imposed when 
this thing is installed and write a DoC that lists them. The rational is that 
we know and understand the requirements they just can't be verified on a 
subassembly.
So I might indicate this is a nonfunctional assembly but list the EMC, Safety, 
and RoHS etc directives that I considered

Or I might indicate it's a non-functional assembly and list only those 
directives that it can comply with at this level. Rather than EMC, safety and 
RoHS, I simply state the RoHS directive for example.

Either of which being the basis for my applying the CE mark.

The CE marking requirements guides don't seem to address this - or I have just 
completely misread them.

Thanks
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