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PTA Balloon Dilatation Catheter - India CDSCO Medical Device Registration

PTA Balloon Dilatation Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000019_000d626a518987b3f0a2d2dbf0637323_e68761e7a46da4827cc11f828b1e1f26. This device is marketed under the brand name Ultraverse® 035 PTA Dilatation 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
PTA Balloon Dilatation Catheter
UID: IMP/MD/2018/000019_000d626a518987b3f0a2d2dbf0637323_e68761e7a46da4827cc11f828b1e1f26

Brand Name

Ultraverse® 035 PTA Dilatation Catheter

Device Class

Class C

Approving Authority

CDSCO

Product Information

The Ultraverse 014 and Ultraverse 018 PTA Dilatation Catheters are recommended for use in Percutaneous transluminal angioplasty (Ultraverse® 035 PTA Dilatation Catheter ) of the renal, popliteal, tibial, femoral, and peroneal arteries. These catheters are not for use in coronary arteries

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