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Angioplasty Kit - India CDSCO Medical Device Registration

Angioplasty Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000082_1f0c88656d8bd168c5eba53250736602_bb2a144b1027d9554e5231fe93377c26. This device is marketed under the brand name MI PAC, PAC-VI. The license holder is Veritas Bioventions Pvt. Ltd, and it is classified as Device Class Class B. The approving authority is Gujarat.

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 B
Angioplasty Kit
UID: MFG/MD/2022/000082_1f0c88656d8bd168c5eba53250736602_bb2a144b1027d9554e5231fe93377c26

Brand Name

MI PAC, PAC-VI

Device Class

Class B

Approving Authority

Gujarat

Product Information

Console kit / PTCA Kit is used during the Angioplasty /PTCA procedures to diagnose / treat cardiac blockages

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