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Rapamycin Target Eluting Coronary Stent System - India CDSCO Medical Device Registration

Rapamycin Target Eluting Coronary Stent System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000008_3fba776a36a187f3455d08ebc1c9c9c2_75ab8f55706e3aca6a7e705f3f7b9cf1. This device is marketed under the brand name Vestasync Sirolimus Eluting Coronary Stent System. The license holder is PURPLE MICROPORT CARDIOVASCULAR PRIVATE LIMITED, and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, Ahmedabad.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class D
Rapamycin Target Eluting Coronary Stent System
UID: MFG/MD/2019/000008_3fba776a36a187f3455d08ebc1c9c9c2_75ab8f55706e3aca6a7e705f3f7b9cf1

Brand Name

Vestasync Sirolimus Eluting Coronary Stent System

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

The Rapamycin Target Eluting Coronary Stent System is indicated for improving coronary luminal diameter in patients with symptomatic heart disease due to de novo native coronary artery lesions length โ‰ค60 mm with reference vessel diameters of โ‰ฅ2.25 to โ‰ค4.0 mm

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