In message
<617eb8c8634c9149aa66c853d7b8ac53040e4...@by2prd0310mb389.namprd03.prod.o
utlook.com>, dated Tue, 26 Feb 2013, "Crane, Lauren"
<lauren.cr...@kla-tencor.com> writes:
The unique aspect of the problem here is that the "unique DoC" issue
seems embedded in the New Legislative Frame (NLF) legislation, the
ideas of which are being promulgated across all CE marking directives
one by one. If you squash it in RTTE it will still pop up in LVD unless
the NLF gets changed.
The NLF Regulation 765/2008 doesn't mention DoC, and the body of the NLF
Decision 768/2008 clearly does not require each item to have its own
DoC. The DoC is always referred to as 'DoC of the product type' (or
'product model').
The problem appears to arise in the loose wording of Annex III of the
Decision:
ANNEX III
EC DECLARATION OF CONFORMITY
1. No … (unique identification of the product):
What does 'product' mean here? The individual item or the 'product type'
or 'product model'.
Since the body of the Decision always refers to the product type or
model, and ***doesn't require a copy of the DoC to accompany every
individual item***, it seems impossible to interpret point 1 of the
Annex to mean other than the (unique) 'model number' or 'sales code' or
'catalogue number' of the product type.
--
OOO - Own Opinions Only. See www.jmwa.demon.co.uk
SHOCK HORROR! Dinosaur-like DNA found in chicken and turkey meals
John Woodgate, J M Woodgate and Associates, Rayleigh, Essex UK
-
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