Hip replacement implant component-Liner(Modular Dual Mobility Insert )
- UID
- IMP/MD/2019/000088_e248bb719275779976252712610129e0_07098a3db5075e466000107cfeef103c
- Device class
- Class C
- Brand name
- Trident II Acetabular Component System
- License holder
- Stryker India Pvt. Ltd.,
- Approving authority
- CDSCO
- Product information
- The indications for use for total hip arthroplasty include: 3. Noninflammatory degenerative joint disease including osteoarthritis and avascular necrosis; 4. Rheumatoid arthritis; 5. Correction of functional deformity; 6. Revision procedures where other treatments or devices have failed; and, 7. Treatment of on-union, femoral neck and trochanteric fractures of the proximal femur with head 8. involvement that are unmanageable using other techniques. 9. Dislocation risks
Hip replacement implant component-Liner(Modular Dual Mobility Insert ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000088_e248bb719275779976252712610129e0_07098a3db5075e466000107cfeef103c. This device is marketed under the brand name Trident II Acetabular Component System. The license holder is Stryker India Pvt. Ltd.,, and it is classified as Device Class Class C. The approving authority is CDSCO.
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