Home GUDID 00819251029452
Tibial Insert Trial, PS-Post, Klassic ONE
Primary DI 00819251029452
Brand Tibial Insert Trial, PS-Post, Klassic ONE
Company TOTAL JOINT ORTHOPEDICS, INC.
Model 2254.02.024
Device description Tibial Insert Trial,PS-Post, size 2, 24mm
Published 2021-10-20
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 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 00819251029452 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 00819251029452 00819251029452 819251029452 0819251029452
GMDN Terms# Term, Definition table Term Definition Knee tibia prosthesis trial A copy of a final tibia prosthesis designed to be used during unicompartmental knee replacement surgery or total knee arthroplasty (TKA) to determine the correct alignment, size, and fit of the final prosthesis. It is one of a set, or a set, of graduated sizes, and may be used in conjunction with a knee femur trial prosthesis and a patella trial prosthesis. It is typically made of metal or polymer material and includes tibial base plate trials, tibial spacer trials, tibial insert trials, tibial stem trials, tibial wedge/augment trials, and guide pin trials. 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 Knee System should be stored in a clean, dry location at room
temperature Special Storage Condition, Specify 0 0 The Klassic Knee 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 00810094692698 Modular Frog Eyes 2263.00.000 2026-06-09 00810094692704 Distal Femoral Cut Block Connector 2174.00.000 2026-06-09 00810094692797 Tibial Reamer, Square Tip, Klassic ONE 25/50mm 2264.00.000 2026-06-09 00810094692933 Magnet Spacer, 5mm 2027.00.000 2026-06-09 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
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