Home GUDID 00843575120441 Kosmo Femoral Hip System
Primary DI 00843575120441
Brand Kosmo Femoral Hip System
Company B-ONE ORTHO, CORP.
Model 8819040010
Catalog number 8819040010
Device description Neck Trial, High Offset, 135°, 43mm
Published 2025-04-07
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 JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented MEH Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented Orthopedic 2 LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented Orthopedic 2 MEH Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00843575120441 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 00843575120441 00843575120441 843575120441 0843575120441
GMDN Terms# Term, Definition table Term Definition Femoral stem prosthesis trial A copy of a final femoral stem prosthesis designed to be used for trial reductions during hip arthroplasty to judge the correct offset, leg-length, and range of motion of the final femoral prosthesis to be implanted. It is one of a set, or a set, of graduated sizes, and is used in conjunction with femoral head trial prostheses. It is typically made of metal or polymer material and includes trial stems, trial sleeves, and trial necks. This is a reusable device intended to be sterilized prior to use.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 081315444 Device count 1 Lot or batch true Manufacturing 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 00843575127143 MOBIO™ Total Knee System 8821331109 8821331109 2026-03-06 00843575127150 MOBIO™ Total Knee System 8821331110 8821331110 2026-03-06 00843575127167 MOBIO™ Total Knee System 8821331111 8821331111 2026-03-06 00843575127174 MOBIO™ Total Knee System 8821331113 8821331113 2026-03-06 00843575127181 MOBIO™ Total Knee System 8821331116 8821331116 2026-03-06 00843575127198 MOBIO™ Total Knee System 8821331119 8821331119 2026-03-06 00843575127204 MOBIO™ Total Knee System 8821331122 8821331122 2026-03-06 00843575127211 MOBIO™ Total Knee System 8821331125 8821331125 2026-03-06 00843575127228 MOBIO™ Total Knee System 8821331309 8821331309 2026-03-06 00843575127235 MOBIO™ Total Knee System 8821331310 8821331310 2026-03-06 00843575127242 MOBIO™ Total Knee System 8821331311 8821331311 2026-03-06 00843575127259 MOBIO™ Total Knee System 8821331313 8821331313 2026-03-06 00843575127266 MOBIO™ Total Knee System 8821331316 8821331316 2026-03-06 00843575127273 MOBIO™ Total Knee System 8821331319 8821331319 2026-03-06 00843575127280 MOBIO™ Total Knee System 8821331322 8821331322 2026-03-06 00843575127297 MOBIO™ Total Knee System 8821331325 8821331325 2026-03-06 00843575127303 MOBIO™ Total Knee System 8821331509 8821331509 2026-03-06 00843575127310 MOBIO™ Total Knee System 8821331510 8821331510 2026-03-06 00843575127327 MOBIO™ Total Knee System 8821331511 8821331511 2026-03-06 00843575127334 MOBIO™ Total Knee System 8821331513 8821331513 2026-03-06
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