Home GUDID 00190376472065 Calibrate
Primary DI 00190376472065
Brand Calibrate
Company ALPHATEC SPINE, INC.
Model 258-06186020
Device description LTX TRIAL, 6 x 18 x 60 mm, 20°
Published 2023-01-05
Public version status New
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 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 00190376472065 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 00190376472065 00190376472065 190376472065 0190376472065
GMDN Terms# Term, Definition table Term Definition Spinal implant trial A copy of a final spinal prosthesis, graft, or other implantable spinal device (e.g., may include intervertebral disc prosthesis, spinal cage, spinal hook) used to validate the proper size of the permanent implant required by the patient, to determine its appropriate position, and/or to verify that the implant site has been cut to the proper dimensions. It can be made of metal or plastic. This is a reusable device.
Device Sizes# Type, Value, Unit table Type Value Unit Angle 20 degree Height 6 Millimeter Length 60 Millimeter Width 18 Millimeter
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 602465783 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 00843511102852 Omnia Medical TiBrid™-TS OMNIA MEDICAL, LLC MAX 2026-08-18 00843511102869 Omnia Medical TiBrid™-TS OMNIA MEDICAL, LLC MAX 2026-08-18 00843511102876 Omnia Medical TiBrid™-TS OMNIA MEDICAL, LLC MAX 2026-08-18 00843511102883 Omnia Medical TiBrid™-TS OMNIA MEDICAL, LLC MAX 2026-08-18 00843511102890 Omnia Medical TiBrid™-TS OMNIA MEDICAL, LLC MAX 2026-08-18 00843511102906 Omnia Medical TiBrid™-TS OMNIA MEDICAL, LLC MAX 2026-08-18 00843511102913 Omnia Medical TiBrid™-TS OMNIA MEDICAL, LLC MAX 2026-08-18 00843511102920 Omnia Medical TiBrid™-TS OMNIA MEDICAL, LLC MAX 2026-08-18 00193982141097 HEDRON GLOBUS MEDICAL, INC. PHM 2026-08-14 00193982141097 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141103 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141103 HEDRON GLOBUS MEDICAL, INC. PHM 2026-08-14 00193982141110 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141110 HEDRON GLOBUS MEDICAL, INC. PHM 2026-08-14 00193982141127 HEDRON GLOBUS MEDICAL, INC. PHM 2026-08-14 00193982141127 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141134 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141134 HEDRON GLOBUS MEDICAL, INC. PHM 2026-08-14 00193982141141 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141141 HEDRON GLOBUS MEDICAL, INC. PHM 2026-08-14 00193982141158 HEDRON GLOBUS MEDICAL, INC. PHM 2026-08-14 00193982141158 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141165 HEDRON GLOBUS MEDICAL, INC. PHM 2026-08-14 00193982141165 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141172 HEDRON GLOBUS MEDICAL, INC. PHM 2026-08-14 00193982141172 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141189 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14 00193982141189 HEDRON GLOBUS MEDICAL, INC. PHM 2026-08-14 00193982141196 HEDRON GLOBUS MEDICAL, INC. PHM 2026-08-14 00193982141196 HEDRON GLOBUS MEDICAL, INC. MAX 2026-08-14