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Austin Moore Endoprothesis - India CDSCO Medical Device Registration

Austin Moore Endoprothesis is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000193_ca2711fe51512bf97f22d6a2c2144cf7_a02958a4e8f3cc946ac014b26145b042. This device is marketed under the brand name MPI. The license holder is Med Plus India, and it is classified as Device Class Class C. 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 C
Austin Moore Endoprothesis
UID: MFG/MD/2019/000193_ca2711fe51512bf97f22d6a2c2144cf7_a02958a4e8f3cc946ac014b26145b042

Brand Name

MPI

License Holder

Med Plus India

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

one piece Endoprothesis replacement component, which is intended for cemented use only, Femoral head and neck fracture Aseptic neurosis of femoral head Osteo, rheumatoid, post traumatic arthritis of hip with minimal accetabular involvement

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