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Cobalt Chromium Peripheral stent - India CDSCO Medical Device Registration

Cobalt Chromium Peripheral stent is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000110_179904cad838c9907db89ba3231063b6_01cf24534eea5138778bc298f6381e92. This device is marketed under the brand name Zephyr , Rejuvant. The license holder is Sahajanand Laser Technology Limited, and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, Ahmedabad.

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
Cobalt Chromium Peripheral stent
UID: MFG/MD/2019/000110_179904cad838c9907db89ba3231063b6_01cf24534eea5138778bc298f6381e92

Brand Name

Zephyr , Rejuvant

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

Intended for the treatment of de novo or restenotic atherosclerotic lesions in peripheral arteries ,renal arteries, palliation in malignant structure in biliary tree

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