I
Illuminatus
First Question: A contract manufacturer makes a medical device for a customer. That device is low risk and self certified. The contract manufacturer places the CE mark on the device for the customer... should they place a CE mark on the outer packaging label? In most cases the shippers are opened up for further processing at the customer's facility.
Another question - a company distributes a self certified device. The device is sold in packs of, say, 25. Each package has a label. Each shipper has a label. Do one, both, or neither of these labels require a CE mark?
Thanks very much for your help and any discussion resulting.
Another question - a company distributes a self certified device. The device is sold in packs of, say, 25. Each package has a label. Each shipper has a label. Do one, both, or neither of these labels require a CE mark?
Thanks very much for your help and any discussion resulting.