Hello all,

I have a new (for me, at least) question.  I have a team looking at
providing a passive external speaker option to one of our ITE systems.  

Are there any specific directives or standards that one needs to consider in
Europe v/v CE-marking?  For instance, does a passive speaker fall under the
EMC directive?  I know that higher power pro audio systems are not allowed
to use 'binder post' connections and that they tend to use bicon connectors
in Europe, but I don't know what standard and/or directive is requiring
this.

Any help is greatly appreciated.

Best regards,

Dave Osborn
Philips Medical Systems
Cardiac and Monitoring Systems
Secretary, ISO TC 121/SC3
[email protected]
+ 1 978 659 3178
fax +1 978 685 5624 

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