Bone screw
- UID
- MFG/MD/2019/000085_38dd9160e1dff87270cbde32ec4a5a30_64c4b20f3ee2c74310a826a1e8e4a980
- Device class
- Class C
- Brand name
- Seinser/Actose/Rootsure/Joibis
- License holder
- Pehchan Pharmaceuticals And Surgicals LLP
- Approving authority
- Central Drug Standards Control Organization, Ahmedabad
- Product information
- The Bone Screw is intended for internal fixation of fractures and reconstruction of bones including the Scapula, Olecranon, Humerus, Radius, Ulna, Pelvis, Distal, Tibia, Fibula, Hand and Foot in adults and for long bones in adolescents in whom the growth plates are fused. It can be used with or without the plates
Bone screw is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000085_38dd9160e1dff87270cbde32ec4a5a30_64c4b20f3ee2c74310a826a1e8e4a980. This device is marketed under the brand name Seinser/Actose/Rootsure/Joibis. The license holder is Pehchan Pharmaceuticals And Surgicals LLP, 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.