Bone Screw
- UID
- MFG/MD/2022/000248_34f5cf5637c17f0474ebe7d8d7cfcaeb_7d1c5b8550f11e7ba6993cdfd20eb00f
- Device class
- Class C
- Brand name
- AOSYS
- License holder
- M/s AOSYS PRIVATE LIMITED
- Approving authority
- Central Drug Standards Control Organization, Ahmedabad
- Product information
- The implants will be used for selected fractures elsewhere in the body so long as medically indicated and bone mass compatible. Bone Screw is intended for implantation into prepared bone during orthopaedic surgery when the surgeon determines the need for additional fixation: bone reconstruction, osteotomy, arthrodesis, joint fusion, fracture repair, and fracture fixation, appropriate for the size of the device
Bone Screw is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000248_34f5cf5637c17f0474ebe7d8d7cfcaeb_7d1c5b8550f11e7ba6993cdfd20eb00f. This device is marketed under the brand name AOSYS. The license holder is M/s AOSYS PRIVATE LIMITED, 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.