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Peripheral Balloon Catheter - India CDSCO Medical Device Registration

Peripheral Balloon Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000014_ab5a7647434535b5ea9b2dbb3838de8e_0783da27428c5a5f01e350647d33d47b. This device is marketed under the brand name CROSSER CTO Recanalization Catheter. The license holder is Bard India Healthcare Pvt. Ltd., and it is classified as Device Class Class C. 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 C
Peripheral Balloon Catheter
UID: IMP/MD/2018/000014_ab5a7647434535b5ea9b2dbb3838de8e_0783da27428c5a5f01e350647d33d47b

Brand Name

CROSSER CTO Recanalization Catheter

Device Class

Class C

Approving Authority

CDSCO

Product Information

The RIVALยฎ PTA Dilatation Catheter is intended to dilate stenoses in the peripheral arteries, treat obstructive lesions of native or synthetic A-V fistulae, and/or re-expand endoluminal stent graft elements in the iliac arteries.

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