CR-PS Knee System - Femoal - India CDSCO Medical Device Registration
CR-PS Knee System - Femoal is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000423_7072a2ec406889934f333b6a18d3cb62_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.
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Brand Name
PFC Sigma
License Holder
Johnson & Johnson Private LimitedDevice Class
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
Knee System - Stem
Brand: PFC Sigma
Johnson & Johnson Private Limited
Knee Replacement System- Femoral
Brand: PFC Sigma
Johnson & Johnson Private Limited
Knee Replacement System- Tibial Insert
Brand: PFC Sigma
Johnson & Johnson Private Limited
CR-PS Knee System - Inserts
Brand: PFC Sigma
Johnson & Johnson Private Limited
C-Section Kit
Brand: PROLENE*
Coronary Artery Bypass Graft
Brand: PROLENE*
Coronary Artery Bypass Graft
Brand: PROLENE*
NON-STERILE NON-ABSORBABLE SURGICAL SUTURE U.S.P.
Brand: BLACK BRAIDED SILK
Coronary Artery Bypass Graft(ETHICON* CABG KIT)
Brand: PROLENE*
NON ABSORBABLE SURGICAL SUTURE U. S. P.
Brand: PROLENE*
NON ABSORBABLE SURGICAL SUTURE U. S. P.
Brand: BLACK BRAIDED SILK
NON ABSORBABLE SURGICAL SUTURE U. S. P.
Brand: PROLENE*
ABHY-ADV KIT
Brand: PROLENE*
Hernia Kit
Brand: PROLENE*