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BONEWAX - India CDSCO Medical Device Registration

BONEWAX is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2020/000136_c9f6538d7a4129567384f712280fdca8_7bf4465f80fb65b6a2cf67735e2f4a20. The license holder is Futura Surgicare Pvt Ltd, and it is classified as Device Class Class C. The approving authority is Sub Zonal Bangalore.

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
BONEWAX
UID: MFG/MD/2020/000136_c9f6538d7a4129567384f712280fdca8_7bf4465f80fb65b6a2cf67735e2f4a20

Device Class

Class C

Approving Authority

Sub Zonal Bangalore

Product Information

General orthopedics, craniomaxillofacial and cardio-thoracic surgery for sternal closure

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