In message <d250d01e39356a4e9cc3b4b459d6655094dc1...@ms-cda-01.advanced-input.com>, dated Tue, 2 Apr 2013, "McInturff, Gary" <[email protected]> writes:

Does one just state there are no requirements at this level on the DoC, do they reference the appropriate directives for safety and EMC for the final product.

If it's not usable on its own, it may well be something that should not have a CE mark and a DoC. From 1.2 of the 'EMC Guide' 2010:

1.2 Defining the scope of apparatus
The EMC Directive defines "apparatus" as any finished appliance, or
combination thereof made commercially available (i.e. placed on the
market) as a single functional unit, intended for the end-user, and liable to generate electromagnetic disturbance, or the performance of which is liable to be affected by such a disturbance.

1.2.1 Finished appliances
A finished appliance is any device or unit that delivers a function and
has its own enclosure.
A finished appliance is considered as apparatus in the sense of the EMC
Directive, if it is intended for the end-user and thus has to fulfil all the applicable provisions of the Directive.
When the finished appliance is intended exclusively for an industrial
assembly operation for incorporation into other apparatus, it is not
apparatus in the sense of the EMC Directive and consequently the EMC
Directive does not apply.

We custom design bits and pieces for end customers in EU, and we keep dancing around this issue both for ITE and medical devices.

End customers are presumably manufacturers, not 'end-users' as defined in the Directive? If not, 1.2.3 of the Guide is applicable:

1.2.3 Components/Sub-assemblies
In contrast to finished appliances, components /sub-assemblies do not, in general, have a proper enclosure intended for their final use. Components/sub-assemblies are often intended to be fitted into or added to an apparatus in order to add an additional function.

1.2.3.1 Components/sub-assemblies within scope
Components or sub-assemblies on the market which are:
- for incorporation into an apparatus by the end-user;
- available to end-users;
are to be considered as apparatus with regard to the application of the
EMC Directive.
The instructions for use accompanying the component or sub-assembly
should include all relevant information, and should assume that
adjustments or connections can be performed by an end-user not aware of
the EMC implications.
Illustrative examples:
Plug-in cards for computers;
Programmable logic controllers;
Electric motors (except for induction motors, see section 1.1.4);
Computer disk drives;

It might have a digital clock but no way to measure emissions until it's in the final enclosure. The end user would then do some final declarations and issue DoC's.

So the 'end-user' in your terminology IS a manufacturer and NOT an end-user in the meaning given in the Directive.

We make RoHS and WEEE statements but those are not currently part of our DoC for EU
Just what does a DoC for a rock look like if I wanted to ship it?

If it's not suitable for throwing, it is benign and thus exempt.
--
OOO - Own Opinions Only. Try www.jmwa.demon.co.uk and www.isce.org.uk
They took me to a specialist burns unit - and made me learn 'To a haggis'.

John Woodgate, J M Woodgate and Associates, Rayleigh, Essex UK

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