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Hemi Arthroplasty - India CDSCO Medical Device Registration

Hemi Arthroplasty is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2020/000271_7c26054054171d2a07943347d45d80a4_c577a4e0fd8eb3dfac79b013f82f2d68. This device is marketed under the brand name Jayon, Ostrio. The license holder is Jayon Implants Pvt Ltd, and it is classified as Device Class Class C. The approving authority is Central Drug Standard Control Organisation, South Zone.

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
Hemi Arthroplasty
UID: MFG/MD/2020/000271_7c26054054171d2a07943347d45d80a4_c577a4e0fd8eb3dfac79b013f82f2d68

Brand Name

Jayon, Ostrio

Device Class

Class C

Approving Authority

Central Drug Standard Control Organisation, South Zone

Product Information

The prosthesis is composed of a metal stem that fits into the hollow marrow space of the thighbone (Jayon, Ostrio). It also has a metal ball that fits into the socket of the hip joint (Jayon, Ostrio). Hemi means half and it is not a total joint replacement, a hemi arthroplasty is generally used to treat a fractured hip

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