Revision Knee Components - Stemmed Tibial Base Plate(Evolve - Stemmed Tibial Base Plate )
- UID
- MFG/MD/2018/000063_fd50d98457b606c71ad42aee6ea41210_c0011b9a1b1b06c5ce56806780866d68
- Device class
- Class C
- Brand name
- PCK Components
- License holder
- Meril Healthcare Pvt. Ltd.
- Approving authority
- Central Drug Standards Control Organization, Ahmedabad
- Product information
- Stemmed Tibial Components are designed to be used with Total Knee System, and is indicated for the following: • Severe knee joint pain, loss of mobility, and disability due to: rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis. • Correction of functional deformities. Post-traumatic loss of knee joint contour, particularly when there is patellofemoral erosion, dysfunction, and/or prior patellectomy. • Moderate valgus, varus, or flexion trauma. • Knee fractures untreatable by other methods • Revision surgery where sufficient bone stock and soft tissue integrity are present These Components are intended for cemented use only. This device is for single use only
Revision Knee Components - Stemmed Tibial Base Plate(Evolve - Stemmed Tibial Base Plate ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2018/000063_fd50d98457b606c71ad42aee6ea41210_c0011b9a1b1b06c5ce56806780866d68. This device is marketed under the brand name PCK Components. The license holder is Meril Healthcare Pvt. Ltd., and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, Ahmedabad.
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.