FDA officials have not issued any certificates to manufacturers of Class II medical devices. The so-called FDA certificates are all counterfeit. The manufacturer provides a 510k number, which can be checked on the FDA official website.
According to the news published by the European Commission on its official website on April 3, 2020, the European Commission will delay the application of the "Medical Device Regulation" (MDR) originally scheduled to come into effect on May 26, 2020, and
At this special time when COVID-19 continues to spread around the globe, in order to support more effectively the response of the international community to the global public health crisis, measures on reinforcing quality regulation over supplies for COV