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Pick 5
My company produces several kinds of borderline medical devices, most of which are listed to 61010-1 2nd edition. When the 3rd edition becomes mandatory for assumption of compliance to the Low Voltage Directive (Oct 2013), how do I show compliance when most of my models are listed to particulars which have not been uplifted to 2nd edition?
If a product is listed to a particular (i.e. 61010-2-010 or 61010-2-051) can I update to 61010-1 3rd edition?
If a product is listed to a particular (i.e. 61010-2-010 or 61010-2-051) can I update to 61010-1 3rd edition?