Home GUDID 04026575392247
Endo-Model SL Knee Prosthesis System
Primary DI 04026575392247
Brand Endo-Model SL Knee Prosthesis System
Company WALDEMAR LINK GmbH & Co. KG
Model 16-2821/22
Catalog number 16-2821/22
Device description Femoral Component,intracondylar, with patellar flange
Published 2015-11-01
Public version status Update
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 JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented KRO Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer LWJ Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented Orthopedic 2 KRO Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer Orthopedic 2 LWJ Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented Orthopedic 2 LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 04026575392247 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 04026575392247 04026575392247 4026575392247
GMDN Terms# Term, Definition table Term Definition Uncoated knee femur prosthesis, metallic An implantable device designed to replace the femoral condyles (femoral 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 tibial and, if required, patellar prosthetic components of the knee joint and its implantation is intended to be performed with bone cement.
Regulatory Flags# DUNS number 315675488 Device count 1 DM exempt true Serial number true Expiration date on label true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 04026575448678 MobileLink Acetabular Cup System 183-353/40 183-353/40 2026-07-09 04026575448685 MobileLink Acetabular Cup System 183-363/40 183-363/40 2026-07-09 04026575448760 MobileLink Acetabular Cup System 183-354/40 183-354/40 2026-07-09 04026575448777 MobileLink Acetabular Cup System 183-355/40 183-355/40 2026-07-09 04026575448784 MobileLink Acetabular Cup System 183-356/40 183-356/40 2026-07-09 04026575448791 MobileLink Acetabular Cup System 183-364/40 183-364/40 2026-07-09 04026575448807 MobileLink Acetabular Cup System 183-365/40 183-365/40 2026-07-09 04026575448814 MobileLink Acetabular Cup System 183-366/40 183-366/40 2026-07-09 04026575448821 MobileLink Acetabular Cup System 183-373/40 183-373/40 2026-07-09 04026575448838 MobileLink Acetabular Cup System 183-374/40 183-374/40 2026-07-09 04026575448845 MobileLink Acetabular Cup System 183-375/40 183-375/40 2026-07-09 04026575448852 MobileLink Acetabular Cup System 183-376/40 183-376/40 2026-07-09 04026575448869 MobileLink Acetabular Cup System 183-743/40 183-743/40 2026-07-09 04026575448876 MobileLink Acetabular Cup System 183-744/40 183-744/40 2026-07-09 04026575448883 MobileLink Acetabular Cup System 183-745/40 183-745/40 2026-07-09 04026575448890 MobileLink Acetabular Cup System 183-746/40 183-746/40 2026-07-09 04026575348213 SPII Model Lubinus 128-950/35 128-950/35 2015-11-01 04026575348220 SPII Model Lubinus 128-951/35 128-951/35 2015-11-01 04026575348237 SPII Model Lubinus 128-952/35 128-952/35 2015-11-01 04026575348244 SPII Model Lubinus 128-953/35 128-953/35 2015-11-01
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