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Structural Heart Devices Market 2021-2027 with Major Key Player: , Medtronic, Jude Medical, Braile Biomedica, Medical Technolog, & more – KSU

Structural Heart Devices Market 2021-2027 with Major Key Player: , Medtronic, Jude Medical, Braile Biomedica, Medical Technolog, & more – KSU
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FDA Grants Micro Interventional Devices, Inc. Breakthrough Device Designation for the MIA-T Percutaneous Tricuspid Annuloplasty System

NEWTOWN, Pa., May 27, 2021 /PRNewswire/ Micro Interventional Devices (MID) has received Breakthrough Device Designation from the U.S. Food and Drug Administration (FDA) for its MIA-T Percutaneous ....

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FDA Grants Micro Interventional Devices, Inc. Breakthrough Device Designation for the MIA™-T Percutaneous Tricuspid Annuloplasty System

/PRNewswire/ Micro Interventional Devices (MID) has received Breakthrough Device Designation from the U.S. Food and Drug Administration (FDA) for its MIA™-T. ....

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Prosthetic Heart Valve Market to Witness Growth Acceleration During 2026

Prosthetic Heart Valve Market to Witness Growth Acceleration During 2026
Prosthetic Heart Valve Market to Witness Growth Acceleration During 2026
BriefingWire.com, 5/06/2021 -
Market Scenario
Global Prosthetic Heart Valve market is expected to reach USD 8,392 Bn by 2026 at a CAGR of 9.5 % during the forecast period.
The Global Prosthetic Heart Valve market is segmented based on type, end user region.
By Product type - transcatheter valve, tissue heart valves, mechanical valve.
By End User â Hospitals, Ambulatory Surgical Centers. By region - North America & South America, Europe, Asia-Pacific and, Middle East & Africa
The prosthetic heart valve is a medical device that implants in the heart disease patient who is suffering from heart failure. The mechanism of this device is that heart valve consists of orifices, which are provided blood flow. ....

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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. ....

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