Home GUDID 00887517567208
CoRoent
Primary DI 00887517567208
Brand CoRoent
Company Nuvasive, Inc.
Model 5164340
Device description CoRoent Ant TLIF PEEK, 16x14x34mm 0°
Published 2015-10-24
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Product Codes# Code, Name table Code Name MAX Intervertebral fusion device with bone graft, lumbar MQP SPINAL VERTEBRAL BODY REPLACEMENT DEVICE ODP Intervertebral fusion device with bone graft, cervical OVE Intervertebral fusion device with integrated fixation, cervical PHM Intervertebral fusion device with bone graft, thoracic
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class MAX Intervertebral Fusion Device With Bone Graft, Lumbar Orthopedic 2 MQP Spinal Vertebral Body Replacement Device Orthopedic 2 ODP Intervertebral Fusion Device With Bone Graft, Cervical Orthopedic 2 OVE Intervertebral Fusion Device With Integrated Fixation, Cervical Orthopedic 2 PHM Intervertebral Fusion Device With Bone Graft, Thoracic Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00887517567208 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00887517567208 00887517567208 887517567208 0887517567208
GMDN Terms# Term, Definition table Term Definition Metallic spinal fusion cage, non-sterile A non-sterile device intended to help fuse segments of the spine to treat anatomical abnormalities of the vertebrae, typically due to degenerative intervertebral disks [i.e., degenerative disc disease (DDD)]. The device is typically designed as a small, hollow and/or porous, threaded or fenestrated cylinder (or other geometric form) made of metal [usually titanium (Ti)] that is implanted between the bones or bone grafts of the spine, to provide mechanical stability and sufficient space for therapeutic spinal bone fusion to occur. Disposable devices associated with implantation may be included. This device must be sterilized prior to use.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 053950783 Device count 1 Lot or batch true Sterilization required before use true Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 08800043966040 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966057 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966064 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966071 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966088 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966095 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966101 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966118 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966125 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966132 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966149 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966156 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966163 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966170 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966187 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966194 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966200 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966217 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966224 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966231 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966248 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966255 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966262 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966279 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966286 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966293 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966309 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966316 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966323 N/A TDM Co., Ltd. MAX 2026-06-08 08800043966330 N/A TDM Co., Ltd. MAX 2026-06-08