Hi Steve:
First, one of my clients has been told by their 3rd party NRTL that a ground
bond test is required as part of factory/production routine tests, even though
it is not required by 61010-1. I have never run into this requirement in my
work history and I would be interested in
Group,
I've not been able to find anything that suggests that the EU DoC can be
provided with the product electronically for a medical device. I sent
an inquiry to the commission and received no response. The MDD and MDR
require that the DoC is shipped with each product and I have a
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