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Orthopaedic Implant- Base - India CDSCO Medical Device Registration

Orthopaedic Implant- Base is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000454_a0d08b7e4060e6e66e04eaf8a472c3f2_63990f01e74ba0f05720fd34f2a38e0e. 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- Base
UID: IMP/MD/2019/000454_a0d08b7e4060e6e66e04eaf8a472c3f2_63990f01e74ba0f05720fd34f2a38e0e

Brand Name

Corail

Device Class

Class D

Approving Authority

CDSCO

Product Information

REEF system is intended for use in total hip arthroplasty only. Total hip arthroplasty is intended to provide increased patient mobility and reduce pain by replacing the damaged hip joint articulation in patients where proximal bone condition is not sufficient and distal anchorage is required to obtain primary stability. REEF system is intended for cementless use only.

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