Dear colleagues,

This questions might have been asked before. Still looking for answers...

Our company purchases power distribution equipment designed per our specs.
This equipment is not put on the market, but integrated in our products, and
does safety/EMC functions(EMI filtering, protection, emergency stop) among
other things, in accordance to the EC Directives applicable to our product.
We believe there is no point to have it CE marked but only compliant with
the standards we need. The text of the EMC Directive reads "the manufacturer
may subcontract certain operations, e.g., apparatus design or production,
provided that he retains overall control and responsibility for the
apparatus as a whole. By the same token, he may use ready-made items or
components, CE marked or not, to produce the apparatus without losing his
status as a manufacturer."

We follow the Technical Construction File route for CE marking.  What's the
documentation required from our sub-contractors that proves compliance with
the EN standards we indicate? Do we need complete copies of test reports,
technical description, analysis, or just a statement of compliance would do
the job? What's the legal value of such a paper in North-America? As we
don't control their production (parts, quality, etc,) what's the
documentation we shall request to ensure all production units are compliant?
What's the industry/your practice in this case?


Alexandru Guidea
CAE Inc.
Montreal, CANADA





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