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Cervical Interbody Fusion Device - India CDSCO Medical Device Registration

Cervical Interbody Fusion Device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000005_c3c015109fe13afcb800015fbf869284_bd517096bc5d039c34bc7ce1a3ec59af. This device is marketed under the brand name CREO. The license holder is M/s Globus Medical India Pvt. Ltd., and it is classified as Device Class Class C. 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 C
Cervical Interbody Fusion Device
UID: IMP/MD/2019/000005_c3c015109fe13afcb800015fbf869284_bd517096bc5d039c34bc7ce1a3ec59af

Brand Name

CREO

Device Class

Class C

Approving Authority

CDSCO

Product Information

Intended for use in skeletally mature patients with degenerative disc disease (CREO) of the cervical spine (CREO) at one or more contiguous levels

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