The European Union Medical Device Directive (MDD) had been in place for almost 25 years before it was replaced by the new European Union Medical Device Regulation (MDR), issued in 2017. This previous directive constituted the EU framework for medical devices, but it did not include in vitro diagnostic medical devices.
However, it was determined that a fundamental revision of those directives was necessary to establish a more robust, transparent, sustainable, and predictable regulatory framework. The intent was to improve the overall level of health and safety of medical devices, while still supporting innovation in the industry.
Jinhua Huacheng Medical Appliance Co.,Ltd.
Manufactuer of disposable medical products: Electrosurgical pencil,grounding plate,skin stapler and ECG electrode
