Home GUDID 00810094690038 Platform Hooded Acetabular Insert Trial
Primary DI 00810094690038
Brand Platform Hooded Acetabular Insert Trial
Company TOTAL JOINT ORTHOPEDICS, INC.
Model 1228.46.032
Device description Hooded Acetabular Insert Trial, 32mm head, size 46mm
Published 2022-09-28
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 LXH Orthopedic manual surgical instrument
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class LXH Orthopedic Manual Surgical Instrument Orthopedic 1
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00810094690038 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 00810094690038 00810094690038 810094690038 0810094690038
GMDN Terms# Term, Definition table Term Definition Acetabulum prosthesis trial, prefabricated, reusable A copy of a final acetabular prosthesis designed to be used for trial reductions during hip arthroplasty to judge the correct size and position of the final acetabular prosthesis to be implanted. It is one of a set, or a set, of graduated sizes, is typically made of metal or polymer material and may be designed in the form of cages, shells, augments, or inserts. This is a reusable device intended to be sterilized prior to use.
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0
Storage And Handling# Type, Low, High table Type Low High Condition Special Storage Condition, Specify 0 0 The Klassic HD Hip System should be stored in a clean, dry location at room
temperature Special Storage Condition, Specify 0 0 The Klassic HD Hip System should be stored in a clean, dry location at room temperature
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 078416717 Device count 1 Sterilization required before use true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00810094692940 AP Sizer with Short Legs SRI-10050 2026-05-15 00810094692728 CR Femoral Trial, Grit Blasted SRI-10051.01 2026-02-05 00810094692735 CR Femoral Trial, Grit Blasted SRI-10051.02 2026-02-05 00810094692742 CR Femoral Trial, Grit Blasted SRI-10051.03 2026-02-05 00810094692759 CR Femoral Trial, Grit Blasted SRI-10051.04 2026-02-05 00810094692766 CR Femoral Trial, Grit Blasted SRI-10051.05 2026-02-05 00810094692773 CR Femoral Trial, Grit Blasted SRI-10051.06 2026-02-05 00810094692780 CR Femoral Trial, Grit Blasted SRI-10051.07 2026-02-05 00810094692506 Tibial Broach Impactor, Revision 2904.00.000 2025-05-14 00810094692278 Universal Cone Impactor Head 2021.12.012 2025-04-24 00810094692285 Universal Cone Impactor Head 2021.34.018 2025-04-24 00810094692292 Universal Cone Impactor Head 2021.57.024 2025-04-24 00810094691950 Universal Cone Impactor Head, Size 1, 12° 2021.01.012 2024-09-06 00810094691967 Universa Cone Impactor Head, Size 2, 12° 2021.02.012 2024-09-06 00810094691974 Universal Cone Impactor Head, Size 3, 18° 2021.03.018 2024-09-06 00810094691981 Universal Cone Impactor Head, Size 4, 18° 2021.04.018 2024-09-06 00810094691998 Universal Cone Impactor Head, Size 5, 24° 2021.05.024 2024-09-06 00810094692001 Universal Cone Impactor Head, Size 6, 24° 2021.06.024 2024-09-06 00810094692018 Universal Cone Impactor Head, Size 7, 24° 2021.07.024 2024-09-06 00819251021197 Femoral Stem Impactor with Anteversion 1307.00.000 2023-12-11
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