Home GUDID 00843575120373 Kosmo Femoral Hip System
Primary DI 00843575120373
Brand Kosmo Femoral Hip System
Company B-ONE ORTHO, CORP.
Model 8819040003
Catalog number 8819040003
Device description Cement Restrictor Trial, 11.25mm O.D.
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 00843575120373 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 00843575120373 00843575120373 843575120373 0843575120373
GMDN Terms# Term, Definition table Term Definition Surgical implant template, reusable A device designed to determine the appropriate size and placement of a non-dental implant for a patient prior to or during implantation surgery. It is typically available as a graduated set or an individual plate (e.g., a translucent plastic sheet or a cut metal shape) with patterns/sizes corresponding to the size of the implant to be used to aid the surgeon in final selection of implant size, placement, and/or adaption. It is used for, e.g., total- or partial-joint prostheses, bone fracture fixation implants (plates, nails, including skull plate implants) or other types of surgical implants. This is a reusable device.
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 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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