Home GUDID 20195860017085
E3D-A Interbody System
Primary DI 20195860017085
Brand E3D-A Interbody System
Company Evolution Spine LLC
Model 110H-M2019
Catalog number 110H-M2019
Device description HAnano E3D-A Ti ALIF 36 X 26mm 20deg 19mm (P 10mm)
Published 2024-02-13
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 OVD Intervertebral fusion device with integrated fixation, 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 OVD Intervertebral Fusion Device With Integrated Fixation, 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 20195860017085 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 20195860017085 20195860017085
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 in the form of a hollow, porous, threaded and/or fenestrated cylindrical or geometrical 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 included with the device.
Device Sizes# Type, Value, Unit table Type Value Unit Angle 20 degree Depth 26 Millimeter Height 19 Millimeter Width 36 Millimeter
Sterilization Methods# Method table Method Radiation Sterilization
Regulatory Flags# DUNS number 116940934 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 08800043912870 N/A TDM Co., Ltd. MAX 2026-06-02 08800043912887 N/A TDM Co., Ltd. MAX 2026-06-02 08800043912894 N/A TDM Co., Ltd. MAX 2026-06-02 08800043912900 N/A TDM Co., Ltd. MAX 2026-06-02 08800043912917 N/A TDM Co., Ltd. MAX 2026-06-02 08800043912924 N/A TDM Co., Ltd. MAX 2026-06-02 08800043912931 N/A TDM Co., Ltd. MAX 2026-06-02 08800043912948 N/A TDM Co., Ltd. MAX 2026-06-02 08800043912955 N/A TDM Co., Ltd. MAX 2026-06-02 08800043912962 N/A TDM Co., Ltd. MAX 2026-06-02 08800043912979 N/A TDM Co., Ltd. MAX 2026-06-02 08800043912986 N/A TDM Co., Ltd. MAX 2026-06-02 08800043912993 N/A TDM Co., Ltd. MAX 2026-06-02 08800043913006 N/A TDM Co., Ltd. MAX 2026-06-02 08800043913013 N/A TDM Co., Ltd. MAX 2026-06-02 08800043913020 N/A TDM Co., Ltd. MAX 2026-06-02 08800043913037 N/A TDM Co., Ltd. MAX 2026-06-02 08800043913044 N/A TDM Co., Ltd. MAX 2026-06-02 08800043913051 N/A TDM Co., Ltd. MAX 2026-06-02 08800043913068 N/A TDM Co., Ltd. MAX 2026-06-02 08800043913075 N/A TDM Co., Ltd. MAX 2026-06-02 08800043964183 N/A TDM Co., Ltd. MAX 2026-06-02 08800043964190 N/A TDM Co., Ltd. MAX 2026-06-02 08800043964206 N/A TDM Co., Ltd. MAX 2026-06-02 08800043964213 N/A TDM Co., Ltd. MAX 2026-06-02 08800043964220 N/A TDM Co., Ltd. MAX 2026-06-02 08800043964237 N/A TDM Co., Ltd. MAX 2026-06-02 08800043964244 N/A TDM Co., Ltd. MAX 2026-06-02 08800043964251 N/A TDM Co., Ltd. MAX 2026-06-02 08800043964268 N/A TDM Co., Ltd. MAX 2026-06-02