A marking applied to products that must fulfill an EC directive for sale in the European Economic Area. For medical devices, the CE Marking follows the Medical Devices Directive, which contain the medical safety standard EN60601-1 and medical EMC standard EN60601-1-2 (which in turn are based on the international standard IEC60601-1).

			A mark for medical devices established by TÜV Rheinland of Germany that shows conformance with the medical safety standards EN60601-1 and EN60601-1-2. TÜV/GM is based on the European Union Medical Device Directive (MDD) EN60601-1.

			A mark from the TÜV Rheinland certiication body that shows compliance with the American and Canadian UL and CSA standards. For medical standards, this mark shows the product meets the requirements of UL2601-1 and CSA C22.2 No.601-1.