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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/2021/000761_5d0fcd7650ac7df53305ead665c5e0ce_d7f55a80aa37a0fbd5f8ad14a40fc1c5. This device is marketed under the brand name Ultraverse 035 PTA Dilatation Catheter . The license holder is Becton Dickinson India Private Limited, 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/2021/000761_5d0fcd7650ac7df53305ead665c5e0ce_d7f55a80aa37a0fbd5f8ad14a40fc1c5

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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