noboost4you and I have been having a lengthy discussion via PM on CE marking to the PED (97/23/EC) and something came up that neither of us are very clear on at this point....
Let's say I'm an American manufacturer of a pressure accessory (not a safety device).
I have a customer who incorporates my pressure accessory into an assembly.
That customer is also an American manufacturer, but sells the assembly to the EU.
What is my responsibility under the PED?
Other information: If I was to sell the accessory directly to the EU I would at most be Category I, Module A (CE mark, self assessment). Most likely it would SEP - no CE mark required.
Let's say I'm an American manufacturer of a pressure accessory (not a safety device).
I have a customer who incorporates my pressure accessory into an assembly.
That customer is also an American manufacturer, but sells the assembly to the EU.
What is my responsibility under the PED?
Other information: If I was to sell the accessory directly to the EU I would at most be Category I, Module A (CE mark, self assessment). Most likely it would SEP - no CE mark required.