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CR-PS Knee System - Inserts - India CDSCO Medical Device Registration

CR-PS Knee System - Inserts is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000423_2d9b4b4c85e7a8f32e47f9b916f3dc54_9aef46acae2aa36a532fb424b4b896d6. This device is marketed under the brand name PFC Sigma. 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
CR-PS Knee System - Inserts
UID: IMP/MD/2019/000423_2d9b4b4c85e7a8f32e47f9b916f3dc54_9aef46acae2aa36a532fb424b4b896d6

Brand Name

PFC Sigma

Device Class

Class D

Approving Authority

CDSCO

Product Information

It is Indicated for total knee replacement include patients with a severely painful and/or severely disabled joint resulting from osteoarthritis, post-traumatic arthritis, rheumatoid arthritis, or a failed previous implant

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