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Balloon Expandable Coronary Stent System - Cobalt Chromium (Prozeta - Balloon Expandable Coronary Stent System - Cobalt Chromium ) - India CDSCO Medical Device Registration

Balloon Expandable Coronary Stent System - Cobalt Chromium (Prozeta - Balloon Expandable Coronary Stent System - Cobalt Chromium ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000295_f0c353ec806c4b55b3fa1b282fea6c3c_b7a9d40ce5ecafe36e730b1b5ec323b4. This device is marketed under the brand name Non-Sterile. The license holder is M/s Vascular Concepts Ltd., and it is classified as Device Class Class D. The approving authority is CDSCO.

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CDSCO Registered
Class Class D
Balloon Expandable Coronary Stent System - Cobalt Chromium (Prozeta - Balloon Expandable Coronary Stent System - Cobalt Chromium )
UID: IMP/MD/2021/000295_f0c353ec806c4b55b3fa1b282fea6c3c_b7a9d40ce5ecafe36e730b1b5ec323b4

Brand Name

Non-Sterile

Device Class

Class D

Approving Authority

CDSCO

Product Information

The Prozeta Coronary Stent System is indicated for use in patients with symptomatic ischemic heart disease due to discrete de novo coronary artery lesions with a reference vessel diameter ranging from 2.0mm to 4.0mm (Non-Sterile) and is intended for treatment of coronary arteries

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