Home GUDID 00888480588535 Reficio DBM Paste
Primary DI 00888480588535
Brand Reficio DBM Paste
Company EBI, LLC
Model 20700321
Published 2015-10-19
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 00888480588535 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 00888480588535 00888480588535 888480588535 0888480588535
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 050410323 Device count 1 HCT/P true 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 00880304820852 Biomet SpinalPak / OrthoPak 106130-22 106130-22 2016-06-07 00812301020188 Biomet SpinalPak / OrthoPak 106130-12 106130-12 2014-09-19 00812301020201 Biomet SpinalPak / OrthoPak 106130-20 106130-20 2014-09-19 00812301020515 Biomet EBI Bone Healing System 1068226 1068226 2014-09-19 00888480588528 Reficio DBM Paste 20700221 2015-10-19 00888480588542 Reficio DBM Paste 20700421 2015-10-19 00888480588559 Reficio DBM Plus 20800521 2015-10-19 00888480588566 Reficio DBM Plus 20900321 2015-10-19 00888480588573 Reficio DBM Plus 20900421 2015-10-19 00888480588580 Reficio DBM Plus 20900521 2015-10-19 00887868269264 Biomet SpinalPak Non-invasive Spine Fusion Stimulator System 1067716-45 1067716-45 2019-02-28 00887868269271 Biomet SpinalPak Non-invasive Spine Fusion Stimulator System 1067716-63 1067716-63 2019-02-28 00887868269288 Biomet SpinalPak Non-invasive Spine Fusion Stimulator System 1067716-72 1067716-72 2019-02-28 00887868269295 Biomet OrthoPak Non-invasive Bone Growth Stimulator System 1067718-45 1067718-45 2019-02-28 00887868269301 Biomet OrthoPak Non-invasive Bone Growth Stimulator System 1067718-63 1067718-63 2019-02-28 00887868269318 Biomet OrthoPak Non-invasive Bone Growth Stimulator System 1067718-72 1067718-72 2019-02-28 00880304820845 Biomet SpinalPak / OrthoPak 106130-14 106130-14 2016-06-07 00812301020010 EBI OsteoGen Implantable Bone Growth Stimulator 10-1318 10-1318 2014-09-19 00812301020027 EBI OsteoGen™ Implantable Bone Growth Stimulator 10-1320 10-1320 2014-09-19 00812301020034 EBI OsteoGen™ Implantable Bone Growth Stimulator 10-1320M 10-1320M 2014-09-19
Other Devices Sharing Product Codes# 
biomet.com