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Vascular Reconstruction Device - India CDSCO Medical Device Registration

Vascular Reconstruction Device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000236_89ebc02df6d024249a3f673317b07013_7e017c93a8cfc3a6ae562cb166b38907. This device is marketed under the brand name Stent. The license holder is Johnson & Johnson Private Limited, 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
Vascular Reconstruction Device
UID: IMP/MD/2020/000236_89ebc02df6d024249a3f673317b07013_7e017c93a8cfc3a6ae562cb166b38907

Brand Name

Stent

Device Class

Class D

Approving Authority

CDSCO

Product Information

The Enterprise 2 Vascular Reconstruction Device is intended for use with occlusive devices in the treatment of intracranial aneurysms

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