RIck,

You ask (your points preceeded with a '>'):
> For some reason, it is still unclear in my mind the role of a competent 
body in the big
> picture. Please bear with me as I ask this question one last time.

> If company A in Europe buys a product from company B in the US, and the 
product
> is delivered with a CE Mark on the device(s). (Of course with the DoC
> accompanying the mark). Shouldn't company A be allowed to determine if the
> equipment suits them for their application AND shouldn't company A be able 
to
> accept whatever equipment they want WITHOUT a competent body involved?  I
> understand that if no standard exists or has been officially published in 
the OJ, a
> competent body might be useful. But in my scenario, I am providing ITE 
equipment
> to a larger system which is arguably in this gray area.

As one who has proceeded through the competent body avenue recently, your 
points touched on some close issues with me. Here's my slant on this. The 
products that my employer provides to our European customers are basically 
ITE with some telco I/O thrown in. These are open systems with MANY possible 
configuration scenarios. By working with a competent body, we were able to 
test a determined single representative "worst case" configuration. Testing 
was performed here in the USA with the competent body playing the part of a 
review authority. This scenario worked well for us. This approach was also 
instrumental in obtaining the NEMKO safety approval without having to retest 
at a NEMKO approved EMC lab.

However, compliance to the EMC Directive must be attested via a CE marking 
and the MDofC. Suitable emissions and immunity standards, specific or 
generic, must be selected for this purpose as your product(s) relate to 
them.

In an open "free market", company A should be allowed to determine if the 
equipment from company B suits them for their application. Your question 
suggesting that "company A be able to accept whatever equipment they want 
WITHOUT a competent body involved" is possible. Simply put, if the products 
being supplied are not contained in the above stated categories and are not 
radio devices, then they fall to the self-declaration route.

> Even here I have some concerns. The final application is a flight 
simulator with
> hydraulic motion platforms, displays, and computer systems. It is not 
obvious to me
> that this is justification for hiring a competent body to evaluate EMC 
performance.

It is my opinion that, aside from the condition of Article 10-2, competent 
body selection is purely optional and voluntary to anyone or any 
organization wishing to do so.

> The issue of "light" industrial Vs "heavy" industrial in my mind is one of
> ruggedization for the effects of EMC. Given that EN55022 defines the 
environment
> for a Class A emission device, the generic immunity standard EN50082-X 
should
> be a customers decision.

You are correct in that the "light" vs"heavy" industrial environments is 
only a matter of EMC ruggedness. This is reflected in Article 4(b) of the 
EMC Directive. In fact, determining which environment should depend soley on 
the characteristics of a product's final intended operating environment. I 
feel this is not so much regulatory, but one of dependability and 
reliability.

> Please excuse me if this is a dumb question, but if someone can shed a bit 
more
> light I promise to shut up on this issue.

I firmly believe that the only dumb question is the one not asked. By not 
asking, it only keeps one and possibly others in the dark. And, dark is one 
thing we don't need more of.

I hope that my opinions expressed here have shed some, or any, light for 
you. Please bear in mind that these opinions are my own.

Best regards,
Ron Pickard
[email protected]

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