Pure Global

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/2020/000472_5d0fcd7650ac7df53305ead665c5e0ce_52a0ff089eccde67268aacce90e27990. This device is marketed under the brand name Ultraskin. The license holder is M/s LepuCare (India) Vascular Solutions Pvt. Ltd.,, and it is classified as Device Class Class D. 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class D
PTA Balloon Dilatation Catheter
UID: IMP/MD/2020/000472_5d0fcd7650ac7df53305ead665c5e0ce_52a0ff089eccde67268aacce90e27990

Brand Name

Ultraskin

Device Class

Class D

Approving Authority

CDSCO

Product Information

PTA balloon catheter is indicated for percutaneous transluminal angioplasty (Ultraskin) in patients with obstructive disease of peripheral arteries, i.e. subclavian, iliac, femoral, popliteal, tibial, and renal arteries

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing