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Nitinol Stent System - India CDSCO Medical Device Registration

Nitinol Stent System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2022/000413_d3f45bd0320504207a059bd641665ff3_6e05089c04736a3129d7cad73ce796aa. This device is marketed under the brand name VISTA BRITE TIP. The license holder is Cardinal Health Medical Products India Pvt Ltd, and it is classified as Device Class Class D. 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 D
Nitinol Stent System
UID: IMP/MD/2022/000413_d3f45bd0320504207a059bd641665ff3_6e05089c04736a3129d7cad73ce796aa

Brand Name

VISTA BRITE TIP

Device Class

Class D

Approving Authority

CDSCO

Product Information

The Cordis PRECISE PRO RX Nitinol Stent System is indicated for use in patients with stenotic lesions of the carotid artery(VISTA BRITE TIP).

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