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CDSCO UID IMP/MD/2019/000005_c3c015109fe13afcb800015fbf869284_bd517096bc5d039c34bc7ce1a3ec59af

Cervical Interbody Fusion Device

M/s Globus Medical India Pvt. Ltd.·Device Class Class C·India CDSCO·Brand: CREO
Registration details
UID
IMP/MD/2019/000005_c3c015109fe13afcb800015fbf869284_bd517096bc5d039c34bc7ce1a3ec59af
Device class
Class C
Brand name
CREO
License holder
M/s Globus Medical India Pvt. Ltd.
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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About this record

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.

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