Home GUDID 07630345706676 M-Vizion Femoral Revision System Extension
Primary DI 07630345706676
Brand M-Vizion Femoral Revision System Extension
Company Medacta International SA
Model 01.22.10.0790
Device description Curved broach L220 ø 21
Published 2026-09-21
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx false
OTC false
Sterile false
Single use false Product Codes# Code, Name table Code Name KWY Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented KWZ Prosthesis, hip, constrained, cemented or uncemented, metal/polymer LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented Orthopedic 2 KWZ Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer Orthopedic 2 LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 07630345706676 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 07630345706676 07630345706676 7630345706676
GMDN Terms# Term, Definition table Term Definition Orthopaedic surgical procedure kit, non-medicated, reusable A collection of various orthopaedic surgical instruments, dressings and the necessary materials intended to be used to perform an orthopaedic surgical procedure, however the kit is not dedicated to orthopaedic implantation. It does not contain pharmaceuticals. This is a reusable device.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 488227125 Device count 1 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label true Expiration date on label false Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 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 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 07630542728563 M-Vizion Femoral Revision System Extension 01.22.10.0779 2026-09-21 07630542728570 M-Vizion Femoral Revision System Extension 01.22.10.0780 2026-09-21 07630542734670 M-Vizion Femoral Revision System Extension 01.22.099 2026-09-21
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