In message <9b1d91af667d4c0aa644f9023fb69...@tamuracorp.com>, dated Tue,
2 Apr 2013, Brian Oconnell <oconne...@tamuracorp.com> writes:
From this side of the pond and from my experience, components for use
by other mfrs in med and ITE have two principle requirements that would
be looked at by the governmental people - the CE mark on the component
and the declaration. If the governmental person goes further,
... you might be censured for putting the CE mark and producing a DoC
for a product that is exempt. Please look at the REGULATION (EC) No
765/2008 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL:
2. The CE marking as presented in Annex II shall be affixed
only to products to which its affixing is provided for by specific
Community harmonisation legislation, and shall not be affixed
to any other product.
--
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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