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Revision stem - India CDSCO Medical Device Registration

Revision stem is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000211_06d25ccdba7cbbce1f35ec5de2108307_811c790491d7b7ebc01c224cbaaf21e1. The license holder is Perfect Medicare Products, and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, Ahmedabad.

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
Revision stem
UID: MFG/MD/2022/000211_06d25ccdba7cbbce1f35ec5de2108307_811c790491d7b7ebc01c224cbaaf21e1

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

intended for use in hip arthroplasty

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