Home GUDID 00843575120991 Kosmo Femoral Hip System
Primary DI 00843575120991
Brand Kosmo Femoral Hip System
Company B-ONE ORTHO, CORP.
Model 8810422280
Catalog number 8810422280
Device description Proportional Offset Collarless Hip Stem 132°, Size 10, For Cemented Use Only
Published 2025-04-07
Public version status New
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 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 00843575120991 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 00843575120991 00843575120991 843575120991 0843575120991
GMDN Terms# Term, Definition table Term Definition Uncoated hip femur prosthesis, modular A sterile implantable principal component of a total hip prosthesis (femoral component) typically designed to replace the femoral head and neck; the device is composed of two or more separate pieces (e.g., head, neck, and stem) designed to be joined and is not coated with materials intended to improve fixation and stability by promoting bone ingrowth. The device may be made of metal and/or ceramic materials. Fixation devices for implantation (e.g., screws and bolts) may be included and implantation is intended to be performed with bone cement.
Regulatory Flags# DUNS number 081315444 Device count 1 Lot or batch true Expiration date on label true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00843575106445 MOBIO™ Total Knee System 8821333209 8821333209 2026-05-29 00843575106452 MOBIO™ Total Knee System 8821333210 8821333210 2026-05-29 00843575106469 MOBIO™ Total Knee System 8821333211 8821333211 2026-05-29 00843575106476 MOBIO™ Total Knee System 8821333213 8821333213 2026-05-29 00843575106483 MOBIO™ Total Knee System 8821333216 8821333216 2026-05-29 00843575106490 MOBIO™ Total Knee System 8821333219 8821333219 2026-05-29 00843575106506 MOBIO™ Total Knee System 8821333222 8821333222 2026-05-29 00843575106513 MOBIO™ Total Knee System 8821333225 8821333225 2026-05-29 00843575106520 MOBIO™ Total Knee System 8821343209 8821343209 2026-05-29 00843575106537 MOBIO™ Total Knee System 8821343210 8821343210 2026-05-29 00843575106544 MOBIO™ Total Knee System 8821343211 8821343211 2026-05-29 00843575106551 MOBIO™ Total Knee System 8821343213 8821343213 2026-05-29 00843575106568 MOBIO™ Total Knee System 8821343216 8821343216 2026-05-29 00843575106575 MOBIO™ Total Knee System 8821343219 8821343219 2026-05-29 00843575106582 MOBIO™ Total Knee System 8821343222 8821343222 2026-05-29 00843575106599 MOBIO™ Total Knee System 8821343225 8821343225 2026-05-29 00843575107619 MOBIO™ Total Knee System 8829302009 8829302009 2026-05-29 00843575107626 MOBIO™ Total Knee System 8829302010 8829302010 2026-05-29 00843575107633 MOBIO™ Total Knee System 8829302011 8829302011 2026-05-29 00843575107640 MOBIO™ Total Knee System 8829302013 8829302013 2026-05-29
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