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Self-expanding peripheral stent system - India CDSCO Medical Device Registration

Self-expanding peripheral stent system is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000166_7eca113e3ec538e36c69b18bddacdc32_56935d070165d00d82b905aabd62cf77. This device is marketed under the brand name Nitinol. The license holder is M/s Luminor Medical Devices 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
Self-expanding peripheral stent system
UID: IMP/MD/2020/000166_7eca113e3ec538e36c69b18bddacdc32_56935d070165d00d82b905aabd62cf77

Brand Name

Nitinol

Device Class

Class C

Approving Authority

CDSCO

Product Information

The device is indicated for the treatment of de novo or restenotic atherosclerotic lesions in peripheral arteries located under the aortic arch and to palliate malignant strictures of the biliary tract with a nominal diameter ranging from 4.5 to 9.5 mm

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