Orthopaedic Implant- Screw
- UID
- IMP/MD/2019/000454_216b558b16eac7efcdcdb5911a04dbbb_ee9ea5140d08ad30d1cfd4b697286c83
- Device class
- Class D
- Brand name
- Corail
- License holder
- Johnson & Johnson Private Limited
- Approving authority
- CDSCO
- Product information
- The use of metallic surgical appliances provides the orthopaedic surgeon with a means of bone fixation and helps generally in the management of fractures and reconstructive surgery. These implants are intended as a guide to normal healing and are not intended to replace normal body structure or bear the weight of the body in the presence of incomplete bone healing. Delayed unions or non-unions in the presence of load bearing or weight bearing might eventually cause the implant to break due to metal fatigue. During use all metal surgical implants are subjected to repeated stress which can result in metal fatigue
Orthopaedic Implant- Screw is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000454_216b558b16eac7efcdcdb5911a04dbbb_ee9ea5140d08ad30d1cfd4b697286c83. This device is marketed under the brand name Corail. The license holder is Johnson & Johnson Private Limited, and it is classified as Device Class Class D. The approving authority is CDSCO.
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