RE: CE Marking - Protoypes

[Enci]

Well, I found the guide I was looking for, and the key issue is the
placing on the market or taking into service. The guide clearly states
demonstrating at an exhibition is not considered to be placing on the
market. It also says a notice is required, as descibed below. Therefore the
application of CE Marking or lack thereof is meaningless.

Enci


Prototype, equipments for demostration aren't covered by the EMC or RTTE 
directive.
This is article 8.2 of RTTE a similar article exist in the EMC directive
2. At trade fairs, exhibitions, demonstrations, etc.,
Member States shall not create any obstacles to the
display of apparatus which does not comply with this
Directive, provided that a visible sign clearly indicates
that such apparatus may not be marketed or put into
service until it has been made to comply.
Ciao
Paolo



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Fw: Websites for world-wide requirements

[Jon Griver]

Paul,

I posted this a few days ago, but it only refers to regulatory requirements
for medical equipment:
http://www.ita.doc.gov/td/mdequip/regulations.html

As it's the site of the US Department of Commerce, it may also have
regulatory requirements in any fields.

Regards,


Jon Griver
www.601help.com
The Medical Device Developer's Guide to IEC 60601-1

 Hi,

 I remember there was a relatively recent discussion on the a website that
 can provide the various regulatory requirements and or contacts for each
 country throughout the world.

 Does anyone still have that website address?

 Thanks for your anticipated help.

 REgards,Paul J Smith , Teradyne, Boston

 Go Patriots


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