By PPD I mean 76/211/EEC which has to do with quantity representation and
quantity control. Annex I, section 3.3 describes the "e" requirements,
refering in part to 71/316/EEC
Lauren
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"Brian O'Connell" <[email protected]>
Sent by: [email protected]
05/13/2009 02:59 PM To
<[email protected]>
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Subject
RE: Differences between CE Mark legislations and non CE Mark legislations
Pre-packaged products directive that requires the e mark ?
please explain - I thought that the PPD applied to quantity control and the
'e'mark was for vehicles.
thanks.
From: [email protected] [mailto:[email protected]]On Behalf Of
[email protected]
Sent: Wednesday, May 13, 2009 10:02 AM
To: John Woodgate
Cc: [email protected]
Subject: Re: Differences between CE Mark legislations and non CE Mark
legislations
John,
I disagree. REACH is all about (well at least partly about) imported articles,
substances and preparations (all "products"). It is as much a market access
regulation as MD or EMCD.
As you know RoHS is being proposed to be a CE mark directive in its upcoming
revision.
There are many other directives that also relate to potential products but
don't require CE marking, such as TPED (requires PI marking), Aerosols
Directive (requires upside-down epsilon marking), Prepackaged Products
Directive (requires "e" marking).
My impression is that CE markings tend to be required where consumer sales are
prominently envisioned, and no marking, or other markings are required where
B2B transactions are more prominent.
Regards,
Lauren Crane
Product Regulatory Analyst
Corporate Product EHS Lead
Applied Materials Inc.
Austin, TX 512 272-6540 [#922 26540]
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