JW et al

 

If I were an EU importer, authorized representative or not, I would, and I
think I should be, wary of bringing in a product where the TF was not
available and provided to me before I do.

 

John E Allen

W. London, UK

 

From: John Woodgate [mailto:[email protected]] 
Sent: 02 February 2017 19:16
To: [email protected]
Subject: Re: [PSES] Authorised Representative in EU

 

Is the Blue Guide entirely consistent with the current LVD and EMCD,  which
have a lot of detail about the responsibilities of bodies in the supply
chain?

 

I think the point about the TF not needing to exist until it's asked for is
not explicitly stated, but is a logical consequence of what is stated.

 

With best wishes DESIGN IT IN! OOO - Own Opinions Only

 <http://www.jmwa.demon.co.uk/> www.jmwa.demon.co.uk J M Woodgate and
Associates Rayleigh England

 

Sylvae in aeternum manent.

 

From: Nyffenegger, Dave [mailto:[email protected]] 
Sent: Thursday, February 2, 2017 6:35 PM
To: [email protected]
Subject: Re: [PSES] Authorised Representative in EU

 

Yes it is a bit confusing as the term "authorized" is used for both the
Manufacturer's representative with responsibility for the DoC and placing
the product into the market as well as for the technical file.  Review the
Blue Guide.  Yes, the manufacturer does not have to have an authorized
representative within the EU. 

 

However the entity identified on the DoC as responsible for compiling the
technical file must be located in the EU.  The two could be but are not
required to be the same.  This is so that the EU authorities have someone
with roots in the EU they can contact for the technical file.  Note that the
entity listed on the DoC as responsible for the technical file does not
necessarily need to be the expert on its content and that the file does not
necessarily have to exist as such until the  time that it's requested by EU
authorities.  This is also explained in the Blue Guide I believe if not the
directive itself.

 

-Dave

 

From: Kunde, Brian [mailto:[email protected]] 
Sent: Thursday, February 02, 2017 11:10 AM
To: [email protected]
Subject: [PSES] Authorised Representative in EU

 

A quick question.

 

A manufacturer established outside the EU placing product on the market in
the EU can but does not have to have an authorized representative within the
EU.?  Is this a correct statement?  

 

AND;

The Machinery Directive requires the name and address of the person
authorized to compile the technical file be established in the EU and listed
on the EU DoC. But this  person is not referred to as the "authorized
representative", even though it may be the same person.  This "person"
appears to have no responsibilities other than compiling and making
available the technical file to Authorities within the Member States.   Is
this also True?

 

Confirm that the EMC and LVD directives do not require the person
responsible for compiling the technical file to be within the EU.?  So if
true, the EU DoC from a manufacturer outside the EU declaring only to the
EMC and LVD does not have to list any "person" from within the EU.? Is this
true?

 

It appears that sometimes these two responsibilities get confused.  Or,
maybe it has been confusing only to me. 

 

Thanks

 

The Other Brian

 

  _____  


LECO Corporation Notice: This communication may contain confidential
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by mistake, please destroy it and notify us of the error. Thank you. 


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