Home GUDID 10889981438869
Reef L
Primary DI 10889981438869
Brand Reef L
Company Seaspine Orthopedics Corporation
Model RL4-284520
Catalog number RL4-284520
Device description LATERAL IMPLANT, 23mm X 18mm X 45mm, 20°
Published 2026-01-30
Public version status New
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 10889981438869 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 10889981438869 10889981438869
GMDN Terms# Term, Definition table Term Definition Metal-polymer composite 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 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 device made of a non-bioabsorbable synthetic polymer with a metallic coating 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.
Regulatory Flags# DUNS number 079840876 Device count 1 Lot or batch true Expiration date on label 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