Home GUDID 00880304462144 OSS™ Orthopedic Salvage System
Primary DI 00880304462144
Brand OSS™ Orthopedic Salvage System
Company Biomet Orthopedics, LLC
Model 161079
Catalog number 161079
Published 2015-10-24
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 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER KRO PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented Orthopedic 2 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer Orthopedic 2 KRO Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00880304462144 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 00880304462144 00880304462144 880304462144 0880304462144
GMDN Terms# Term, Definition table Term Definition Diaphysis prosthesis An artificial substitute for the diaphysis (shaft) of a humerus, femur, or tibia intended to be implanted for the long-term stabilization of segmental bone defects (e.g., due to osteomyelitis, trauma, bone tumours, or non-healed fractures after osteosynthesis/revision arthroplasty). It is a modular device that typically includes a resection element (spacer), intramedullary nails (inserted into the intramedullary canal), screws, and connectors all made of metal [e.g., titanium (Ti)]; components are both sterile and non-sterile. Instruments for implantation are typically included and implantation may be performed with or without bone cement.
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0 Device Size Text, specify 0
Regulatory Flags# DUNS number 129278169 Device count 1 Lot or batch true Manufacturing date on label true Expiration date on label true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00880304474185 Arcos® Modular Revision Hip System 11-302102 11-302102 2015-10-24 00880304474246 Arcos® Modular Revision Hip System 11-302101 11-302101 2015-10-24 00880304539259 Arcos® Modular Revision Hip System 11-302109 11-302109 2015-10-24 00889024711280 Jgrknt Reusable Fishmouth Perc Guide SSI008662 SSI008662 2026-08-25 00889024712034 Percutaneous Soft Anchor Short 1.4mm Guide SSI008661 SSI008661 2026-08-25 00880304527386 Active Articulation 010000990 010000990 2020-05-15 00880304527393 Active Articulation 010000991 010000991 2020-05-15 00880304485020 Active Articulation Hip System EP-200144 EP-200144 2015-11-03 00880304485037 Active Articulation Hip System EP-200146 EP-200146 2015-11-03 00880304485044 Active Articulation Hip System EP-200148 EP-200148 2015-10-24 00880304485051 Active Articulation Hip System EP-200150 EP-200150 2015-10-24 00880304485068 Active Articulation Hip System EP-200152 EP-200152 2015-10-24 00880304485075 Active Articulation Hip System EP-200154 EP-200154 2015-10-24 00880304485082 Active Articulation Hip System EP-200156 EP-200156 2015-10-24 00880304485099 Active Articulation Hip System EP-200158 EP-200158 2015-10-24 00880304485105 Active Articulation Hip System EP-200160 EP-200160 2015-10-24 00880304485112 Active Articulation Hip System EP-200162 EP-200162 2015-10-24 00880304485129 Active Articulation Hip System EP-200164 EP-200164 2015-11-04 00880304485136 Active Articulation Hip System EP-200166 EP-200166 2015-10-24 00880304491328 Active Articulation™ Dual Mobility Hip System XL-200144 XL-200144 2015-10-24
Other Devices Sharing Product Codes# 
zimmerbiomet.com