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Vascular Balloon-Expandable Stent System - India CDSCO Medical Device Registration

Vascular Balloon-Expandable Stent System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000076_d1fe1c03d1f12da59175e92fab7f2d07_4d3ca2b728b71ffc7a95423eff29612d. This device is marketed under the brand name 1. WILMA 2. FINCH & 3.PIPIT. The license holder is Sahajanand Medical Technologies 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
Vascular Balloon-Expandable Stent System
UID: MFG/MD/2022/000076_d1fe1c03d1f12da59175e92fab7f2d07_4d3ca2b728b71ffc7a95423eff29612d

Brand Name

1. WILMA 2. FINCH & 3.PIPIT

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

The ILYOFIT Vascular Balloon-Expandable Stent System is indicated for the treatment of de novo and restenotic lesions in atherosclerotic peripheral arteries and in palliative treatment of the biliary tree

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