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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_7909290c949493df59cd12fc7702c949. 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_7909290c949493df59cd12fc7702c949

Brand Name

CROSSER CTO Recanalization Catheter

Device Class

Class C

Approving Authority

CDSCO

Product Information

Atlas PTA Balloon Dilatation Catheters are recommended for use in Percutaneous Transluminal Angioplasty of the iliac arteries and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae. This catheter is not for use in coronary arteries

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