G T.K Medical products awarded CE Certificate under EU-MDR

    G T.K Medical announces it has been awarded European Union Medical Device Regulation (MDR) CE certification for its veress needles, organ collection bag, single-use trocar and single-use minimally invasive surgery surgical instruments. The certification allows G T.K Medical to sell its products throughout the European Economic Area. We are very pleased to have achieved this milestone and it is not only the "green pass" for our products to reach the EU market, but also an important affirmation of product quality, safety and effectiveness.

    CE MDR certification is the latest requirement of European medical device regulations, which ensure the safety and effectiveness of medical devices with higher standards, so the gold content of CE MDR certificate is self-evident.

    With the commitment to continued innovation, G T.K Medical brings safer, more effective and more convenient medical devices to the patients. We are very pleased to bring in the new way to our European Union journey ahead.