Home GUDID 00810094701284 Klassic Tibial Baseplate, Revision
Primary DI 00810094701284
Brand Klassic Tibial Baseplate, Revision
Company TOTAL JOINT ORTHOPEDICS, INC.
Model 6200.05.000
Device description Tibial Baseplate, Revision, Sz 5
Published 2025-05-14
Public version status New
Distribution status In Commercial Distribution
MRI safety MR Conditional
Rx true
Sterile true
Single use true
Product Codes# Code, Name table Code Name JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer OIY Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer Orthopedic 2 OIY Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00810094701284 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 00810094701284 00810094701284 810094701284 0810094701284
GMDN Terms# Term, Definition table Term Definition Uncoated knee tibia prosthesis, metallic An implantable device designed to replace the tibial condyles (tibial component) during primary bicondylar replacement of the knee joint, femoral bone resection, or to replace a dysfunctional knee prosthesis (revision); it is made of metal [e.g., cobalt-chrome (Co-Cr), cobalt-chrome-molybdenum (Co-Cr-Mo), titanium (Ti)] and is not coated with a material intended to improve fixation and stability by promoting bone ingrowth. The device is designed to articulate with an insert and/or the femoral prosthetic component of the knee joint and its implantation is intended to be performed with bone cement.
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
Sterilization Methods# Method table Method Radiation Sterilization
Regulatory Flags# DUNS number 078416717 Device count 1 Lot or batch true Expiration date on label true Sterilization required before use true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00810094692803 Klassic Blade Femoral Broach, Line-To-Line, size 0 SRI-10054.00 2026-07-27 00810094692810 Klassic Blade Femoral Broach, Line-To-Line, size 1 SRI-10054.01 2026-07-27 00810094692827 Klassic Blade Femoral Broach, Line-To-Line, size 2 SRI-10054.02 2026-07-27 00810094692834 Klassic Blade Femoral Broach, Line-To-Line, size 3 SRI-10054.03 2026-07-27 00810094692841 Klassic Blade Femoral Broach, Line-To-Line, size 4 SRI-10054.04 2026-07-27 00810094692858 Klassic Blade Femoral Broach, Line-To-Line, size 5 SRI-10054.05 2026-07-27 00810094692865 Klassic Blade Femoral Broach, Line-To-Line, size 6 SRI-10054.06 2026-07-27 00810094692872 Klassic Blade Femoral Broach, Line-To-Line, size 7 SRI-10054.07 2026-07-27 00810094692889 Klassic Blade Femoral Broach, Line-To-Line, size 8 SRI-10054.08 2026-07-27 00810094692896 Klassic Blade Femoral Broach, Line-To-Line, size 9 SRI-10054.09 2026-07-27 00810094692902 Klassic Blade Femoral Broach, Line-To-Line, size 10 SRI-10054.10 2026-07-27 00810094692919 Klassic Blade Femoral Broach, Line-To-Line, size 11 SRI-10054.11 2026-07-27 00810094692926 Klassic Blade Femoral Broach, Line-To-Line, size 12 SRI-10054.12 2026-07-27 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
Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 00840097536552 iTotal Identity CR 3DP Porous Restor3d, Inc. OIY 2026-07-31 00840097536552 iTotal Identity CR 3DP Porous Restor3d, Inc. JWH 2026-07-31 00840097536569 iTotal Identity CR 3DP Porous Restor3d, Inc. OIY 2026-07-31 00840097536569 iTotal Identity CR 3DP Porous Restor3d, Inc. JWH 2026-07-31 00840097536576 iTotal Identity CR 3DP Porous Restor3d, Inc. OIY 2026-07-31 00840097536576 iTotal Identity CR 3DP Porous Restor3d, Inc. JWH 2026-07-31 00840097536583 iTotal Identity CR 3DP Porous Restor3d, Inc. OIY 2026-07-31 00840097536583 iTotal Identity CR 3DP Porous Restor3d, Inc. JWH 2026-07-31 00840097536590 iTotal Identity CR 3DP Porous Restor3d, Inc. OIY 2026-07-31 00840097536590 iTotal Identity CR 3DP Porous Restor3d, Inc. JWH 2026-07-31 03701089509695 AMPLITUDE AMPLITUDE SAS JWH 2026-07-31 03701089517492 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517508 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517515 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517522 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517539 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517546 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517553 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517560 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517577 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517584 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517591 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517607 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517614 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517621 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517638 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517645 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517652 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517669 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089518390 TRAX AMPLITUDE SAS JWH 2026-07-29