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Sirolimus Eluting Stent System - (Pronova - Sirolimus Eluting Stent System - ) - India CDSCO Medical Device Registration

Sirolimus Eluting Stent System - (Pronova - Sirolimus Eluting Stent System - ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000295_20cef746a960c13466042b8b7ad33ab5_7d6b02ff36175489f29f3540dc52f14c. 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
Sirolimus Eluting Stent System - (Pronova - Sirolimus Eluting Stent System - )
UID: IMP/MD/2021/000295_20cef746a960c13466042b8b7ad33ab5_7d6b02ff36175489f29f3540dc52f14c

Brand Name

Non-Sterile

Device Class

Class D

Approving Authority

CDSCO

Product Information

The Pronova Coronary Stent System is indicated for use in patients with symptomatic ischemic heart disease due to discrete de novo coronary artery lesions (Non-Sterile) with a reference vessel diameter ranging from 2.0mm to 4.0mm (Non-Sterile). Long term outcome for this permanent implant is unknown at present

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