Knee replacement system Femoral component - India CDSCO Medical Device Registration
Knee replacement system Femoral component is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000211_d62c9eff837cd8e6c2866fe0c2975c6f_692cd57dbaef413cdc47002115ba0ead. The license holder is Perfect Medicare Products, and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, Ahmedabad.
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License Holder
Perfect Medicare ProductsDevice Class
Approving Authority
Central Drug Standards Control Organization, Ahmedabad
Product Information
The System for Knee Arthroplasty Constrained is intended to replace the articular surface of the distal femur, proximal tibia and patellar surface during the surgical procedure of total knee joint replacement, performed in circumstances where this joint, in skeletally mature individuals, are impaired as a result of pathologies such as non-inflammatory degenerative joint disease ##PLACEHOLDER_0##, traumatic arthritis, ankylosis of non-infectious origin and knee arthrodesis. The product is indicated for the replacement of the natural joint in primary knee arthroplasty procedures in patients who, according to the clinical evaluation, require medial-lateral, anterior-posterior and varus / valgus totally restricted stabilization due to inadequate function of ligaments needing ##PLACEHOLDER_0## wedges and/or extensions, due to poor quality or absence of bone stock. It is also indicated for the partial or total replacement of components in revision procedures of knee arthroplasty
Knee Replacement system Insert Poly
Hip replacement system Cup
Brand: osteoarthrosis
Knee replacement system Tibia component
Hip replacement system Head
Brand: osteoarthrosis

