RapibSorb Resorbable Fixation System -"The Synthes resorbable plate, mesh, foil, screw and tack system is used for bone fixation in the management of fractures or reconstructions of the craniofacial skeleton and as graft containment. The plates, meshes, foils, screws and tacks should only be used in locations subject to low biomechanical loading, i.e. non- load-bearing osteosynthesis exclusively. Examples of appropriate indications include: – Trauma repair and reconstructive procedures in the mid facial area, maxilla and cranium. – Containment of bone grafts or bone graft substitutes in other parts of the body in non-load-bearing indications.",chronOS Bone Void Filler Implants
- UID
- IMP/MD/2020/000120_0ac0bc93f74636d91edddcb42abe7256_3d0e165ce42a3f4982fd7d200940a937
- Device class
- Class D
- Brand name
- plates
- Approving authority
- CDSCO
- Product information
- The CERVIOS chronOS implants are intended for use as intervertebral body fusion devices in skeletally mature patients with degenerative disease of the cervical spine (plates). The CERVIOS chronOS implants are designed for an anterior approach
RapibSorb Resorbable Fixation System -"The Synthes resorbable plate, mesh, foil, screw and tack system is used for bone fixation in the management of fractures or reconstructions of the craniofacial skeleton and as graft containment. The plates, meshes, foils, screws and tacks should only be used in locations subject to low biomechanical loading, i.e. non- load-bearing osteosynthesis exclusively. Examples of appropriate indications include: – Trauma repair and reconstructive procedures in the mid facial area, maxilla and cranium. – Containment of bone grafts or bone graft substitutes in other parts of the body in non-load-bearing indications.",chronOS Bone Void Filler Implants is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000120_0ac0bc93f74636d91edddcb42abe7256_3d0e165ce42a3f4982fd7d200940a937. This device is marketed under the brand name plates. The license holder is Johnson & Johnson Private Limited ,A-1/ 50, Room No. 2, 100 Shed Area, G.l.D.C., Vapi, Tal Pardi (Valsad) ,Valsad Gujarat ,396195 ,India, and it is classified as Device Class Class D. The approving authority is CDSCO.
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.