Home GUDID 00843575121028 Kosmo Femoral Hip System
Primary DI 00843575121028
Brand Kosmo Femoral Hip System
Company B-ONE ORTHO, CORP.
Model 8810310013
Catalog number 8810310013
Device description Cement Restrictor, Size 3
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 00843575121028 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 00843575121028 00843575121028 843575121028 0843575121028
GMDN Terms# Term, Definition table Term Definition Polymer orthopaedic cement restrictor, non-bioabsorbable A non-bioabsorbable, implantable device designed to be inserted into the medullary canal of a bone (e.g., femur, tibia, or humerus) during orthopaedic surgery to prevent cement progression in the diaphysis and therefore facilitate cement pressurization during the introduction of an implant. It is typically made of polyetheretherketone (PEEK) or ultrahigh molecular weight polyethylene (UHMWPE) and is available in a variety of designs (e.g., straight or tapered, hollow with a fenestrated surface), and it may have a toothed surface to prevent its migration from the desired location. It may incorporate a metal orientation marker for radiographs and it is not intended for spinal application.
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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