Some marking directives specify components, otherwise is Pro-forma -> note
'CE' marks on component power supplies, caps, relays, etc. And these
components will typically have CB reports and/or test certs to EN standards.
All of my customers demand the CE for component power supplies. But that is
ok, because I have test certs and CB reports for the TF.

As for the end-use of an assembly - this is where conditions of
acceptability should be in the report or cert or TF or napkin.

Brian

-----Original Message-----
From: [email protected] [mailto:[email protected]]On Behalf Of McInturff,
Gary
Sent: Friday, December 09, 2011 11:01 AM
To: '[email protected]'
Subject: 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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