The EU Medical Device Regulation has established a unique device identification (UDI) system that is similar to the United States Food and Drug Administration (FDA) system. If a company intends to provide or distribute medical devices into the EU marketplace, the labeling on those products will need to comply with this new UDI system. Compliance with the new MDR regulation is mandatory for medical device companies that intend to sell products in Europe.
Jinhua Huacheng Medical Appliance Co.,Ltd.
Manufactuer of disposable medical products: Electrosurgical pencil,grounding plate,skin stapler and ECG electrode
