Saturday, December 3, 2022


Bioretec Files for CE Mark for its Bioresorbable RemeOs Magnesium Screw in the EU

Bioretec’s target is to receive the CE mark and to introduce the bioresorbable magnesium alloy trauma screw into the markets in the European Union during 2022.

LSO Medical Announces CE Approval of Next-Gen LUMESEAL Laser

Designed to enhance ease-of-use and to provide greater precision and control throughout the procedure, Lumeseal is announced as the successor of the efficient and widely used ENDOTHERME 1470 platform.

Next-Gen LUMESEAL Laser for Treatment of Varicose Vein Receives CE Approval

"The integration of SnakeBack® technology on LUMESEAL® is a big step forward for the development of the technique. Beyond its direct impact on enhancing the reproducibility and comfort of laser delivery, the LUMESEAL® platform allows us to assess further improvements in the EVLT technique (new wavelengths, applicators,) "says M. Rochon, LSO Medical CEO.

CoapTech Receives CE Mark Approval and CPT Procedure Code for Its PUMA-G System

The PUMA System™ is a new category of minimally invasive devices, enabling ultrasound to be used for procedures in hollow organs of the body where previously it was impossible or unsafe to do so.

EG-UC5T Linear Array Endoscope Receives CE Mark Reports SonoScape

EG-UC5T is characterized by its large, 4.0-mm instrument channel and its short rigid distal end, pushing the boundaries of therapeutic excellence.

UNITY-B Percutaneous Balloon Expandable Biodegradable Biliary Stent Receives European CE Mark

The CE mark approval of the UNITY-B Percutaneous Biodegradable implant represents yet another milestone for QualiMed and all the companies of Q3 Medical and our collective mission of Creating Value By Helping People.

By using this website you agree to accept Medical Device News Magazine Privacy Policy