How can a person determine what products need CE marks, and to what directives? Pointers to guidance documents please.
Example: We make medical devices. But of course, we also sell wall brackets, carts, tote bags, interconnect cables, printer paper, batteries and chargers, electrodes and sensors, etc... Which of them need CE marks, and to what directives? I am familiar with the scopes of the Medical Device Directive, the EMC directive, the Low Voltage directive and a couple others. It's what I don't know that can bite me. ___________________ Heber Farnsworth, P.E. Physio-Control Corp, Seattle, USA
