Home GUDID 00887517825100 TLX
Primary DI 00887517825100
Brand TLX
Company Nuvasive, Inc.
Model 1792621
Catalog number 1792621
Device description TLX Implant, 11x11x26mm 20°
Published 2026-04-25
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx false
OTC false
Sterile false
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 00887517825100 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 00887517825100 00887517825100 887517825100 0887517825100
GMDN Terms# Term, Definition table Term Definition Metallic spinal interbody fusion cage A device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery in order to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD). It is typically in the form of a hollow, porous, threaded and/or fenestrated cylindrical, or disc-shaped device made of metal [e.g., titanium (Ti)] that provides mechanical stability and sufficient space for therapeutic spinal bone fusion to occur; bone graft is typically used to help with osseointegration. Fixation screws and devices associated with implantation may be packaged with the cage.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 053950783 Device count 1 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label false Expiration date on label false Donation ID number false Contains natural rubber latex false No natural rubber latex false 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 08800043917301 N/A TDM Co., Ltd. MAX 2026-06-10 08800043917318 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
globusmedical.com