Peripheral Dilatation Catheter - India CDSCO Medical Device Registration

Peripheral Dilatation Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000421_e56e32f9b030b456759caecea650ad6e_3ac0c23fbeab50d96fd8b981fdbc6cde. This device is marketed under the brand name RX Herculink Elite Peripheral Stent System. The license holder is Abbott Healthcare 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.

Free Database

CDSCO Registered

Class Class C

Peripheral Dilatation Catheter

UID: IMP/MD/2018/000421_e56e32f9b030b456759caecea650ad6e_3ac0c23fbeab50d96fd8b981fdbc6cde

Brand Name

RX Herculink Elite Peripheral Stent System

License Holder

Abbott Healthcare Private Limited

Device Class

Class C

Approving Authority

CDSCO

Product Information

The Viatrac 14 Plus Peripheral Dilatation Catheter is intended: • To dilate stenosis in the peripheral arteries (RX Herculink Elite Peripheral Stent System). • For the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae