Home GUDID 07630030803192 MiniMAX Stems
Primary DI 07630030803192
Brand MiniMAX Stems
Company Medacta International SA
Model 01.13.103L
Device description miniMAX Stem - Size 3 Left
Published 2017-08-21
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 KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented LZY Prosthesis, Hip, Hemi-, Femoral, Metal Ball MEH Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented Orthopedic 2 LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented Orthopedic 2 LZY Prosthesis, Hip, Hemi-, Femoral, Metal Ball 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 07630030803192 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 07630030803192 07630030803192 7630030803192
GMDN Terms# Term, Definition table Term Definition Press-fit hip femur prosthesis, one-piece A sterile implantable principal component of a total hip prosthesis (femoral component) designed to replace the femoral head and neck. The device is one-piece and is contoured to enable fixation by pressing the distal end into the cortex of the remaining natural femur to achieve a mechanical interlock without the use of bone cement. The device may be made of metal and/or ceramic materials; supplemental fixation devices for implantation (e.g., screws and bolts) may be included.
Regulatory Flags# DUNS number 488227125 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 07630040795166 Surgical Manual Instrument 02.12.10.0845 2026-09-25 07630542792359 Surgical Manual Instrument 02.12.10.3127 2026-09-25 07630040738767 Surgical Manual Instrument 01.22.10.0051 2026-09-21 07630345706584 M-Vizion Femoral Revision System Extension 01.22.10.0781 2026-09-21 07630345706591 M-Vizion Femoral Revision System Extension 01.22.10.0782 2026-09-21 07630345706607 M-Vizion Femoral Revision System Extension 01.22.10.0783 2026-09-21 07630345706614 M-Vizion Femoral Revision System Extension 01.22.10.0784 2026-09-21 07630345706621 M-Vizion Femoral Revision System Extension 01.22.10.0785 2026-09-21 07630345706638 M-Vizion Femoral Revision System Extension 01.22.10.0786 2026-09-21 07630345706645 M-Vizion Femoral Revision System Extension 01.22.10.0787 2026-09-21 07630345706652 M-Vizion Femoral Revision System Extension 01.22.10.0788 2026-09-21 07630345706669 M-Vizion Femoral Revision System Extension 01.22.10.0789 2026-09-21 07630345706676 M-Vizion Femoral Revision System Extension 01.22.10.0790 2026-09-21 07630345706683 M-Vizion Femoral Revision System Extension 01.22.10.0791 2026-09-21 07630345706690 M-Vizion Femoral Revision System Extension 01.22.10.0792 2026-09-21 07630345706706 M-Vizion Femoral Revision System Extension 01.22.10.0793 2026-09-21 07630345706713 M-Vizion Femoral Revision System Extension 01.22.10.0794 2026-09-21 07630345706720 M-Vizion Femoral Revision System Extension 01.22.10.0795 2026-09-21 07630542702112 Surgical Manual Instrument 01.22.10.0174 2026-09-21 07630542723162 M-Vizion Femoral Revision System Extension 01.22.10.0402 2026-09-21
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