Meril Healthcare Latitud Hemi-Hip Replacement System (Cemented) - HSA Registration DE0501843
Access comprehensive regulatory information for Meril Healthcare Latitud Hemi-Hip Replacement System (Cemented) in the Singapore medical device market through Pure Global AI's free database. This CLASS C medical device is registered under HSA registration number DE0501843 and owned by Meril Healthcare Pvt. Ltd.. The device was registered on July 06, 2018.
This page provides complete registration details including product owner information, registrant details, and regulatory compliance data from the official Singapore HSA medical device database. Pure Global AI offers free access to Singapore's complete medical device registry, helping global MedTech companies navigate HSA regulations efficiently.
The Latitud Hemi-Hip Replacement System is intended for use in hemi-hip arthroplasty. Hemi-hip arthroplasty is performed in patients where there is evidence of a satisfactory natural acetabulum and sufficient femoral bone to fix and support the Femoral Stem. Hemi-hip Arthroplasty is indicated in the following conditions: - Acute traumatic fracture of the femoral head or neck that cannot be appropriately treated with internal fixation. - Fracture dislocation of the hip that cannot be appropriately treated with internal fixation. - Avascular necrosis of femoral head. - Non-union of femoral neck fractures. - Certain high subcapital and femoral neck fractures in the elderly. - Degenerative arthritis involving only the femoral head in which the acetabulum does not require replacement. - Pathology involving only the femoral head/neck and /proximal femur that can be adequately treated by hemi-hip arthroplasty.

