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Void Centrailser-Centraliser - India CDSCO Medical Device Registration

Void Centrailser-Centraliser is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000333_5bc25b3aa584afcc70d39e4cbbfdd294_bea74321891ea2e3dac897ab070ad0de. This device is marketed under the brand name C-Stem. The license holder is Johnson & Johnson Private Limited, and it is classified as Device Class Class D. The approving authority is CDSCO.

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
Void Centrailser-Centraliser
UID: IMP/MD/2019/000333_5bc25b3aa584afcc70d39e4cbbfdd294_bea74321891ea2e3dac897ab070ad0de

Brand Name

C-Stem

Device Class

Class D

Approving Authority

CDSCO

Product Information

It is indicated for severe arthropathy due to advanced rheumatoid or osteo-arthritis where conservative therapy or alternative treatments have failed or are considered unsuitable, arthropathy due to degenerative disease, acute trauma, and a previous failed joint replacement. The patient's joint must be anatomically and structurally suited to receive the selected implant(C-Stem).

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