Medical equipment has both class A and B limits but I’ve keep hearing that for EU in can only be Class B – but I can’t find anything other than rumor to support that. Our equipment must meet class B because of internal requirements so I’ve never really tracked the requirement via standard callout. Can someone direct me to the EU requirement that it must all be Class B? If it is actually a requirement what is the justification?
Gary McInturff Reliability/Compliance Engineer Advanced Input Systems Esterline Corporation 600 West Wilbur Avenue Coeur d' Alene, Idaho 83815 Tel: 208 635 8306 Fax 208 635 8706 - This message is from the IEEE Product Safety Engineering Society emc-pstc discussion list. To post a message to the list, send your e-mail to <[email protected]> All emc-pstc postings are archived and searchable on the web at http://www.ieeecommunities.org/emc-pstc Graphics (in well-used formats), large files, etc. can be posted to that URL. Website: http://www.ieee-pses.org/ Instructions: http://listserv.ieee.org/request/user-guide.html List rules: http://www.ieee-pses.org/listrules.html For help, send mail to the list administrators: Scott Douglas <[email protected]> Mike Cantwell <[email protected]> For policy questions, send mail to: Jim Bacher <[email protected]> David Heald <[email protected]>
