Home GUDID 00850011324110
L-Varlock
Primary DI 00850011324110
Brand L-Varlock
Company SPINESOURCE INC
Model 110
Catalog number VAL-CA-10-09
Device description The L-Varlock is a lumbar cage, for intervertebral body fusion.
Published 2019-11-12
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Single use true Product Codes# Code, Name table Code Name MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class MAX Intervertebral Fusion Device With Bone Graft, Lumbar Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00850011324110 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 00850011324110 00850011324110 850011324110 0850011324110
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 9 Millimeter Width 10 Millimeter
Storage And Handling# Type, Low, High table Type Low High Condition Special Storage Condition, Specify 0 0 store away from light and sunlight
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 150955560 Device count 1 DM exempt true 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