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Intraluminal Support Device - India CDSCO Medical Device Registration

Intraluminal Support Device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000078_ea21d8e78ae044752b24da1104645e60_98451412d99025aca8177c2e54b17b26. This device is marketed under the brand name Flow Re-Direction Endoluminal Device. The license holder is Faith Biotech 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
Intraluminal Support Device
UID: IMP/MD/2021/000078_ea21d8e78ae044752b24da1104645e60_98451412d99025aca8177c2e54b17b26

Brand Name

Flow Re-Direction Endoluminal Device

Device Class

Class D

Approving Authority

CDSCO

Product Information

The LVIS EVO Device is intended for use with embolic coils for the treatment of intracranial neurovascular diseases

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