ARTHROSCOPY IMPLANTS
- UID
- MFG/MD/2021/000156_cabcb89c77bdac0a52fc51fb48bb103e_f46b6a8ab2931caf689887db791c190e
- Device class
- Class C
- Brand name
- ORTHOFLEX MEDISYS INDIA PVT. LTD.
- License holder
- Orthoflex Medisys India Pvt Ltd
- Approving authority
- Central Drug Standards Control Organization, Ahmedabad
- Product information
- Arthroscopy Implants are intended for use in fixation of semitendinous and/or gracile tendon grafts. ACL/PCL Screw is intended for use in anterior/posterior cruciate ligament (ORTHOFLEX MEDISYS INDIA PVT. LTD.) reconstruction procedures. ACL/PCL Screw is indicated for fixation of bone-patellar tendon- bone graft to the femoral/tibial bone drill hole in the anterior cruciate ligament reconstruction, fixation of the soft tissue graft to the femoral/tibial bone drill hole in the anterior cruciate ligament (ORTHOFLEX MEDISYS INDIA PVT. LTD.) reconstruction and reconstruction of posterior cruciate ligament (ORTHOFLEX MEDISYS INDIA PVT. LTD.). The Arthroscope is intended to be used as an endoscope in arthroscopic procedures performed on the knee, shoulder, hip, wrist (ORTHOFLEX MEDISYS INDIA PVT. LTD.), temporal mandibular joint, ankle, elbow, and feet (ORTHOFLEX MEDISYS INDIA PVT. LTD.) to view the surgical site
ARTHROSCOPY IMPLANTS is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2021/000156_cabcb89c77bdac0a52fc51fb48bb103e_f46b6a8ab2931caf689887db791c190e. This device is marketed under the brand name ORTHOFLEX MEDISYS INDIA PVT. LTD.. The license holder is Orthoflex Medisys India Pvt Ltd, and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, Ahmedabad.
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