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HEMl-ENDOPROSTHESIS - India CDSCO Medical Device Registration

HEMl-ENDOPROSTHESIS is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2020/000178_0e8ee9abde75a73ec12b1f1eb56d65f4_f7ded49184070ed70f3b06a168210b39. The license holder is Yogeshwar Implants (I) Pvt Ltd, and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, West Zone.

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CDSCO Registered
Class Class D
HEMl-ENDOPROSTHESIS
UID: MFG/MD/2020/000178_0e8ee9abde75a73ec12b1f1eb56d65f4_f7ded49184070ed70f3b06a168210b39

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

The YIPL Hemi Endoprosthesis are intended to be used by qualified and trained orthopaedic surgeons to carry out a partial or 'hemi' replacement of the femoral head of the hip joint in cases involving degenerative or traumatic changes to the femoral head, where there is x-ray evidence of a satisfactory acetabulum and sufficient bone in the femoral neck to seat the prosthesis with or without bone cement. These devices are meant to bear load while in use and are subjected to various mechanical forces. The extent to which the device would withstand these forces is limited by the operating surgeon achieving appropriate restoration of hip biomechanics and periarticular soft tissues.

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