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 MFG/MD/2020/000118_5d0fcd7650ac7df53305ead665c5e0ce_c3224b25a79235f3289014bca33743b1. The license holder is Relisys Medical Devices Limited, and it is classified as Device Class Class B. The approving authority is Telangana.

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 B
PTA Balloon Dilatation Catheter
UID: MFG/MD/2020/000118_5d0fcd7650ac7df53305ead665c5e0ce_c3224b25a79235f3289014bca33743b1

Device Class

Class B

Approving Authority

Telangana

Product Information

PTA Balloon Dilatation Catheters or HP PTA Balloon Dilatation Catheters, are indicated for Percutaneous Transluminal Angioplasty ##PLACEHOLDER_0## in the peripheral vasculature, iliac, femoral, ilio- femoral, popliteal, infra popliteal, and renal arteries as well as the treatment of obstructive lesions of native and synthetic arteriovenous dialysis fistulae.

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing