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Prosthesis Implant - India CDSCO Medical Device Registration

Prosthesis Implant is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000144_ca4ebb2ec065e59163c87908e4774cca_8d06739ebeb4e420fc1abc1df9cb5f8a. This device is marketed under the brand name RELIFEORTHO. The license holder is RELIFE ORTHO, 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
Prosthesis Implant
UID: MFG/MD/2019/000144_ca4ebb2ec065e59163c87908e4774cca_8d06739ebeb4e420fc1abc1df9cb5f8a

Brand Name

RELIFEORTHO

License Holder

RELIFE ORTHO

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

Prosthesis Implant are used in Proximal femur bone fractures, where is femur proximal area are fractured badly, the surgeon removed proximal area and they fixed endo prosthesis and fix with femur distal part

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