To all, The following scenario is in regards to the EMC Directive.
We are a manufacturer located in the US. We have various products that were placed on the EU market prior to the enforcement of the EMC Directive. We need to repair some of these products. The repairs will not modify the product to an "as new" piece of apparatus. We want to have the products repaired in the US. Questions: 1. Following the repairs, do we need to meet the requirements of the Directive? If so, why? 2. If not, how do we get the products back into the EU without the CE Marking? Hopefully someone has had some experience with this issue. All responses are appreciated. Regards Joe Martin EMC/Product Safety Engineer Applied Biosystems [email protected] ------------------------------------------- This message is from the IEEE EMC Society Product Safety Technical Committee emc-pstc discussion list. Visit our web site at: http://www.ewh.ieee.org/soc/emcs/pstc/ To cancel your subscription, send mail to: [email protected] with the single line: unsubscribe emc-pstc For help, send mail to the list administrators: Ron Pickard: [email protected] Dave Heald: [email protected] For policy questions, send mail to: Richard Nute: [email protected] Jim Bacher: [email protected] All emc-pstc postings are archived and searchable on the web at: http://ieeepstc.mindcruiser.com/ Click on "browse" and then "emc-pstc mailing list"
