Pure Global

Non-compliant PTA Balloon Dilatation Catheter - India CDSCO Medical Device Registration

Non-compliant PTA Balloon Dilatation Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000134_af6882c2cf9162dfe62c8b1c0a9ce3f0_53982f1e36687d4fd7ad9a4e48c1b7c6. This device is marketed under the brand name Introducer Sheath Set. The license holder is Rukman Medical Devices And Equipments 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class C
Non-compliant PTA Balloon Dilatation Catheter
UID: IMP/MD/2019/000134_af6882c2cf9162dfe62c8b1c0a9ce3f0_53982f1e36687d4fd7ad9a4e48c1b7c6

Brand Name

Introducer Sheath Set

Device Class

Class C

Approving Authority

CDSCO

Product Information

The PTA balloon dilatation catheter is intended to dilate stenoses in the iliac, femoral, iliofemoral, popliteal, infrapopliteal, and renal arteries, and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae. This device is also indicated for stent dilatation post-deployment in the peripheral vasculature

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing