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Balloon Dilatation Catheter - India CDSCO Medical Device Registration

Balloon Dilatation Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2018/000028_16eb53f14e746dc332d80db12a830d7a_5c2d1f2d28e0eee9232319225f58ba1d. This device is marketed under the brand name First Brand. The license holder is Meril Life Sciences Pvt. Ltd., 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
Balloon Dilatation Catheter
UID: MFG/MD/2018/000028_16eb53f14e746dc332d80db12a830d7a_5c2d1f2d28e0eee9232319225f58ba1d

Brand Name

First Brand

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

It is indicated for dilatation of native stenotic cardiac valves. It is also indicated for balloon dilatation of the stenotic portion of peripheral vessels and aorta. Further, it is indicated for stenting procedure and pre/post-delivery expansion of stents

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