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Monday, October 25, 2021

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Micro Interventional Devices

Micro Interventional Devices Submits CE Mark Technical Documentation for the MIA-T Percutaneous Tricuspid Annuloplasty System

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.

Micro Interventional Devices, Inc.™ Successfully Treats First-in-Human Patient with Percutaneous MIA™, Minimally Invasive Annuloplasty Technology

"The percutaneous MIA system has the potential to be a safe and effective intervention for patients with moderate to severe tricuspid regurgitation," stated Prof. Audrius Aidieitis, MD.

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