Home GUDID 07630542774041 M-Vizion Femoral Revision System Extension
Primary DI 07630542774041
Brand M-Vizion Femoral Revision System Extension
Company Medacta International SA
Model 01.29.200
Device description MECTACER Head Biolox Delta dia.22.2 12/14-M
Published 2026-09-21
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile true
Single use true 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 07630542774041 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 07630542774041 07630542774041 7630542774041
GMDN Terms# Term, Definition table Term Definition Ceramic femoral head prosthesis An implantable artificial substitute for a diseased or injured femoral head that has an outer surface made of ceramic (e.g., alumina, zirconia). It is designed to be attached to the trunnion of a prosthetic femoral stem/shaft or a head/stem adaptor, and to articulate with an acetabulum prosthesis as part of a total hip arthroplasty (THA) or with a bipolar component as part of a partial hip replacement. The device ranges in form from partially to fully spherical (ball-shaped) and is available in various sizes.
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 true Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false 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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