Home GUDID 00880304532328 COMPREHENSIVE REVERSE SHOULDER INSTRUMENT
Primary DI 00880304532328
Brand COMPREHENSIVE REVERSE SHOULDER INSTRUMENT
Company Biomet Orthopedics, LLC
Model 406206
Catalog number 406206
Published 2016-10-28
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true Product Codes# Code, Name table Code Name KWS PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED PHX shoulder prosthesis, reverse configuration
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented Orthopedic 2 PHX Shoulder Prosthesis, Reverse Configuration Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00880304532328 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 00880304532328 00880304532328 880304532328 0880304532328
GMDN Terms# Term, Definition table Term Definition Surgical drill guide, reusable A manual surgical device designed to simultaneously place, angle, and guide a rotating surgical drill on hard tissue (e.g., bone); some types are also intended for guiding bone-coring instruments (e.g., keel punch). It is designed in a tubular form or with guiding holes and may have serrations at its distal end to enable firm placement on hard tissue surfaces (it is not bored into the tissue); it can have a handle or be held by another device (e.g., orthopaedic jig), and typically allows protection of the surrounding soft tissue during surgery. It is typically made of metal and may have graduations along its length; it is not custom-made for a specific patient. This is a reusable device.
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 129278169 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 00880304474185 Arcos® Modular Revision Hip System 11-302102 11-302102 2015-10-24 00880304474246 Arcos® Modular Revision Hip System 11-302101 11-302101 2015-10-24 00880304539259 Arcos® Modular Revision Hip System 11-302109 11-302109 2015-10-24 00889024711280 Jgrknt Reusable Fishmouth Perc Guide SSI008662 SSI008662 2026-08-25 00889024712034 Percutaneous Soft Anchor Short 1.4mm Guide SSI008661 SSI008661 2026-08-25 00880304527386 Active Articulation 010000990 010000990 2020-05-15 00880304527393 Active Articulation 010000991 010000991 2020-05-15 00880304485020 Active Articulation Hip System EP-200144 EP-200144 2015-11-03 00880304485037 Active Articulation Hip System EP-200146 EP-200146 2015-11-03 00880304485044 Active Articulation Hip System EP-200148 EP-200148 2015-10-24 00880304485051 Active Articulation Hip System EP-200150 EP-200150 2015-10-24 00880304485068 Active Articulation Hip System EP-200152 EP-200152 2015-10-24 00880304485075 Active Articulation Hip System EP-200154 EP-200154 2015-10-24 00880304485082 Active Articulation Hip System EP-200156 EP-200156 2015-10-24 00880304485099 Active Articulation Hip System EP-200158 EP-200158 2015-10-24 00880304485105 Active Articulation Hip System EP-200160 EP-200160 2015-10-24 00880304485112 Active Articulation Hip System EP-200162 EP-200162 2015-10-24 00880304485129 Active Articulation Hip System EP-200164 EP-200164 2015-11-04 00880304485136 Active Articulation Hip System EP-200166 EP-200166 2015-10-24 00880304491328 Active Articulation™ Dual Mobility Hip System XL-200144 XL-200144 2015-10-24
Other Devices Sharing Product Codes# 
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