Home GUDID 00887517679727 CoRoent
Primary DI 00887517679727
Brand CoRoent
Company Nuvasive, Inc.
Model 6081123P2
Device description CoRoent Large MP, 11x9x23mm 8°
Published 2019-08-22
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Sterile true
Single use true Product Codes# Code, Name table Code Name MAX Intervertebral fusion device with bone graft, lumbar 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 PHM Intervertebral Fusion Device With Bone Graft, Thoracic Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00887517679727 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 00887517679727 00887517679727 887517679727 0887517679727
GMDN Terms# Term, Definition table Term Definition Polymeric spinal fusion cage, sterile A 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) and is made of non-bioabsorbable synthetic polymer [e.g., polyetheretherketone (PEEK)] that is implanted between the bones or bone grafts of the spine, to provide mechanical stability and sufficient space for bone fusion to occur. Disposable devices associated with implantation may be included.
Sterilization Methods# Method table Method Radiation Sterilization
Regulatory Flags# DUNS number 053950783 Device count 1 Lot or batch true Manufacturing date on label true Expiration date on label 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 M719GLL100QC0 3DP Lumbar Interbody System Genesys Orthopedics Systems LLC MAX 2026-07-14 M719GLL101QC0 3DP Lumbar Interbody System Genesys Orthopedics Systems LLC MAX 2026-07-14 M719GLL106QC0 3DP Lumbar Interbody System Genesys Orthopedics Systems LLC MAX 2026-07-14 M719GLL107QC0 3DP Lumbar Interbody System Genesys Orthopedics Systems LLC MAX 2026-07-14 08800043913099 N/A TDM Co., Ltd. MAX 2026-06-10 08800043913105 N/A TDM Co., Ltd. MAX 2026-06-10 08800043913112 N/A TDM Co., Ltd. MAX 2026-06-10 08800043913129 N/A TDM Co., Ltd. MAX 2026-06-10 08800043913136 N/A TDM Co., Ltd. MAX 2026-06-10 08800043913143 N/A TDM Co., Ltd. MAX 2026-06-10 08800043913150 N/A TDM Co., Ltd. MAX 2026-06-10 08800043913167 N/A TDM Co., Ltd. MAX 2026-06-10 08800043913174 N/A TDM Co., Ltd. MAX 2026-06-10 08800043913181 N/A TDM Co., Ltd. MAX 2026-06-10 08800043913198 N/A TDM Co., Ltd. MAX 2026-06-10 08800043913204 N/A TDM Co., Ltd. MAX 2026-06-10 08800043913211 N/A TDM Co., Ltd. MAX 2026-06-10 08800043917288 N/A TDM Co., Ltd. MAX 2026-06-10 08800043917295 N/A TDM Co., Ltd. MAX 2026-06-10 00887517729545 TLX Nuvasive, Inc. MAX 2026-04-25 00887517729576 TLX Nuvasive, Inc. MAX 2026-04-25 00887517729620 TLX Nuvasive, Inc. MAX 2026-04-25 00887517729644 TLX Nuvasive, Inc. MAX 2026-04-25 00887517729705 TLX Nuvasive, Inc. MAX 2026-04-25 00887517729767 TLX Nuvasive, Inc. MAX 2026-04-25 00887517729781 TLX Nuvasive, Inc. MAX 2026-04-25 00887517824912 TLX Nuvasive, Inc. MAX 2026-04-25 00887517824912 TLX Nuvasive, Inc. PHM 2026-04-25 00887517824929 TLX Nuvasive, Inc. PHM 2026-04-25 00887517824929 TLX Nuvasive, Inc. MAX 2026-04-25
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