Home GUDID 08800039812061
IVA Cage Ti
Primary DI 08800039812061
Brand IVA Cage Ti
Company DIOMEDICAL CO.,LTD.
Model A
Catalog number TDI.40260620
Device description Lateral Lumbar Interbody Fusion Titanium CageL40 x W26 x H20 x A6
Published 2018-06-19
Public version status Update
Distribution status In Commercial Distribution
MRI safety MR Unsafe
Rx true
Single use true
Product Codes# Code, Name table Code Name MAX Intervertebral fusion device with bone graft, lumbar ODP Intervertebral fusion device with bone graft, cervical
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class MAX Intervertebral Fusion Device With Bone Graft, Lumbar Orthopedic 2 ODP Intervertebral Fusion Device With Bone Graft, Cervical Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 08800039812061 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 08800039812061 08800039812061 8800039812061
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.
Device Sizes# Type, Value, Unit table Type Value Unit Height 20 Millimeter
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 557795909 Device count 1 DM exempt true Lot or batch true Manufacturing 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 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