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Orthopaedic Implant- Screw - India CDSCO Medical Device Registration

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.

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.

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CDSCO Registered
Class Class D
Orthopaedic Implant- Screw
UID: IMP/MD/2019/000454_216b558b16eac7efcdcdb5911a04dbbb_ee9ea5140d08ad30d1cfd4b697286c83

Brand Name

Corail

Device Class

Class D

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

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