Home GUDID 00880304684881 StaGraft DBM Plus
Primary DI 00880304684881
Brand StaGraft DBM Plus
Company Biomet Orthopedics, LLC
Model 92-2007
Catalog number 92-2007
Device description DBM in a Lipid Carrier with Porous Calcium Granules
Published 2015-10-24
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 GXP Methyl Methacrylate For Cranioplasty MBP Filler, Bone Void, Osteoinduction (W/O Human Growth Factor) MQV Filler, Bone Void, Calcium Compound
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class GXP Methyl Methacrylate For Cranioplasty Neurology 2 MBP Filler, Bone Void, Osteoinduction (W/O Human Growth Factor) Orthopedic 2 MQV Filler, Bone Void, Calcium Compound Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00880304684881 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 00880304684881 00880304684881 880304684881 0880304684881
GMDN Terms# Term, Definition table Term Definition Bone matrix implant, human-derived An sterile implantable device made primarily of human demineralized bone matrix (DBM) (acid extraction of allogeneic bone resulting in loss of most of the mineralized component but retention of proteins) intended to fill bony voids or gaps caused by trauma or surgery, including use in the maxillofacial and/or mandibular bone. The device is bioabsorbable, osteoconductive, and has demonstrated at least potential osteoinductivity for the stimulation of new bone growth. The DBM may be combined with various carrier compounds (e.g., gelatin, hydrogel, starch) or other materials. It is available in the form of powder, crushed granules, putty, chips, or a gel that can be injected through a syringe.
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0
Regulatory Flags# DUNS number 129278169 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 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
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