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Aortic Valve Replacement Kit - India CDSCO Medical Device Registration

Aortic Valve Replacement Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000230_972f6c9f32fe9806b5aed8c2bd12f431_c20b99a1e5f2b2421dc3e549d58576ba. This device is marketed under the brand name Bylatoral Femoral Bypass Surgery Kit. The license holder is Lotus Surgical Pvt Ltd, and it is classified as Device Class Class D. The approving authority is CDSCO -North Zone, Ghaziabad.

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
Aortic Valve Replacement Kit
UID: MFG/MD/2019/000230_972f6c9f32fe9806b5aed8c2bd12f431_c20b99a1e5f2b2421dc3e549d58576ba

Brand Name

Bylatoral Femoral Bypass Surgery Kit

Device Class

Class D

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

Intended used for surgical dressing and control blood loss during Aortic valve repair or replacement surgery, is a type of surgery that offers excellent valve function and works in coordination with the entire circulatory system to protect each part from damage

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