Peter, 

The Machinery Directive Guide gives excellent guidance on these sorts of
questions à http://www.cen.eu/cen/Sect
rs/Sectors/Machinery/Documents/guide_ap
lication_directive_2006-42-ec-2nd_edit_6-2010_en.pdf

 

Search on “established outside the EU”.  

 

It can be a tricky point, but a company outside the EU is not really within
reach of the directive. Whoever is importing your products is more directly on
the hook. And DEPENDING ON THE DIRECTIVE IN QUESTION CE marking and DoC’ing
may not be relevant for B2B sales. If your company is not actually planning on
placing your items directly on the EU market or putting them directly into
service, i.e. if they are truly B2B components, you may not need to do much at
all except assure your customers via contract terms that your products have
been designed such that when your customers integrate them, they will not
hinder the compliance of the larger product. 

 

There is no requirement in any directive I know of, that a product be composed
of components that are CE Marked, except for some of the tricky ErP
implementing measures. 

 

Caveats galore – as various customs authorities are playing by their own
rule books regarding component import rules, many people in the game speak
>from “common sense” rather than reading each directive in detail, and
there is still no RoHS II guidance to state with certainty that component EEE
is out of scope. 

-- 
Lauren Crane (mr.) 
Product Regulatory Analyst | Corporate Product EHS | Applied Materials 
Office 512.272.6540 | Mobile 512.736.7201 | America - Europe - Asia 

-external use-  This is my own opinion only and not necessarily that of my
employer. 
** Save paper and trees! Please consider the environment before printing this
e-mail.

 

From: [email protected] [mailto:[email protected]] On Behalf Of
[email protected]
Sent: Friday, August 26, 2011 3:06 PM
To: [email protected]
Subject: CE mark

 

Hello group,

 

We are a US based manufacturer that sells our products to global customer and
some of these individual customers are requesting that we CE mark our products
so that they can integrate them into their system for EU. I have everything
done including my DoC (Declaration of conformity) but we don't have any
importer or sales office in EU and therefore don't know what address I should
use on my DoC. How can a US manufacturer CE complete the DoC and affix the CE
mark on the product when they don't have any present in the EU?

 

Thanks

Peter

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