GIG HARBOR, Wash.--(BUSINESS WIRE)--Generic Medical Devices, Inc.™ (GMD™), the first company to design, develop, manufacture and supply quality surgical products marketed at generic prices, today announced CE Marking and a EC-Declaration of Conformity (EC-DoC) indicating compliance with essential health and safety requirements set out in applicable European Directives that will allow the company to place the GMD Universal Circumcision Clamp on the market in all European Union countries, as well as other countries that accept this certification. In January, GMD announced 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market the circumcision clamp domestically. Today’s announcement opens the door for worldwide sales of the company’s first product and the first generic alternatives to standard-of-care surgical implementation devices.
