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Peripheral Stent System - India CDSCO Medical Device Registration

Peripheral Stent System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000421_2ef8d650c58e699764f154f2102aaf6b_0f246d642a4f6836dd5defa55bc5e776. 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.

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CDSCO Registered
Class Class C
Peripheral Stent System
UID: IMP/MD/2018/000421_2ef8d650c58e699764f154f2102aaf6b_0f246d642a4f6836dd5defa55bc5e776

Brand Name

RX Herculink Elite Peripheral Stent System

Device Class

Class C

Approving Authority

CDSCO

Product Information

The Supera peripheral stent system is indicated for peripheral vascular use following failed percutaneous transluminal angioplasty (RX Herculink Elite Peripheral Stent System) and palliative treatment of biliary strictures produced by malignant neoplasms

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