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Stent Graft Balloon Catheter - India CDSCO Medical Device Registration

Stent Graft Balloon Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000451_bb624807eb3afb4a2b774c2cb2a9c87a_a5e525c9d16f30ce4ea93e42f4672ab4. This device is marketed under the brand name E-xpand. The license holder is Vibgyor Health Care Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is CDSCO.

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
Stent Graft Balloon Catheter
UID: IMP/MD/2019/000451_bb624807eb3afb4a2b774c2cb2a9c87a_a5e525c9d16f30ce4ea93e42f4672ab4

Brand Name

E-xpand

Device Class

Class B

Approving Authority

CDSCO

Product Information

The E-xpand Stent Graft Balloon Catheter has been developed for use with JOTECโ€™s self-expanding endovascular Stent Graft Systems and is designed to facilitate Stent Graft expansion

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