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Micro Interventional Devices, Inc.™ Announces Submission of CE Mark Technical Documentation for the MIA-T™ Percutaneous Tricuspid Annuloplasty System


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NEWTOWN, Pa., Jan. 28, 2021 /PRNewswire/
Micro Interventional Devices, Inc.™ (MID) announced today that it has submitted the required technical documentation for CE Mark approval for its MIA-T™ Percutaneous Tricuspid Annuloplasty System for tricuspid valve repair to its Notified Body. The receipt of a CE Mark would allow MID to commercialize MIA-T in the European Union in countries governed by the European Medical Device Regulations (MDR).  MID is anticipating an approval in 2021.  This will enable a treatment option for millions of patients currently at too high a risk to be treated with the standard of care, open surgical repair with cardiopulmonary bypass. ....

United-states , Katherine-whitman , Michael-whitman , Willard-hennemann , European-union , Company-contact , Interventional-devices-inc , Interventional-devices , Percutaneous-tricuspid-annuloplasty-system , European-medical-device-regulations , Transcatheter-tricuspid-annular-repair , Device-regulation