Home GUDID 00840996173520
HARRIER-SA Lumbar Interbody System
Primary DI 00840996173520
Brand HARRIER-SA Lumbar Interbody System
Company Choice Spine, LP
Model Y070-28362521
Device description HARRIER-SA,TRIAL,28x36x21,25 DEG
Published 2018-07-14
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Product Codes# Code, Name table Code Name MAX Intervertebral fusion device with bone graft, lumbar OVD Intervertebral fusion device with integrated fixation, lumbar
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
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00840996173520 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 00840996173520 00840996173520 840996173520 0840996173520
GMDN Terms# Term, Definition table Term Definition Intervertebral-body internal spinal fixation system A group of sterile implantable devices designed to apply force to a series of vertebrae to correct scoliosis (lateral curvature of the spine) or other spinal conditions. The system components are typically made of medical grade titanium and consists of various vertebral plates that are punched into each of a series of vertebral bodies. An eye-type screw is inserted in a hole in the centre of each plate, and a braided cable is threaded through each eye-type screw. The cable is tightened with a tension device and is fastened or crimped at each eye-type screw.
Device Sizes# Type, Value, Unit table Type Value Unit Depth 28 Millimeter Height 21 Millimeter Width 36 Millimeter
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 078293017 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 00840283403460 LumiVy™ VY SPINE LLC MAX 2026-06-05 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