Primary Device ID | 00888480588542 |
NIH Device Record Key | 8fd236c0-f967-4753-94b4-da8a9e44a9c3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Reficio DBM Paste |
Version Model Number | 20700421 |
Company DUNS | 050410323 |
Company Name | EBI, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | true |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 1-973-299-9300 |
btbs.csorders@biomet.com | |
Phone | 1-973-299-9300 |
btbs.csorders@biomet.com | |
Phone | 1-973-299-9300 |
btbs.csorders@biomet.com | |
Phone | 1-973-299-9300 |
btbs.csorders@biomet.com | |
Phone | 1-973-299-9300 |
btbs.csorders@biomet.com | |
Phone | 1-973-299-9300 |
btbs.csorders@biomet.com | |
Phone | 1-973-299-9300 |
btbs.csorders@biomet.com | |
Phone | 1-973-299-9300 |
btbs.csorders@biomet.com | |
Phone | 1-973-299-9300 |
btbs.csorders@biomet.com | |
Phone | 1-973-299-9300 |
btbs.csorders@biomet.com | |
Phone | 1-973-299-9300 |
btbs.csorders@biomet.com | |
Phone | 1-973-299-9300 |
btbs.csorders@biomet.com | |
Phone | 1-973-299-9300 |
btbs.csorders@biomet.com | |
Phone | 1-973-299-9300 |
btbs.csorders@biomet.com | |
Phone | 1-973-299-9300 |
btbs.csorders@biomet.com | |
Phone | 1-973-299-9300 |
btbs.csorders@biomet.com | |
Phone | 1-973-299-9300 |
btbs.csorders@biomet.com | |
Phone | 1-973-299-9300 |
btbs.csorders@biomet.com | |
Phone | 1-973-299-9300 |
btbs.csorders@biomet.com | |
Phone | 1-973-299-9300 |
btbs.csorders@biomet.com | |
Phone | 1-973-299-9300 |
btbs.csorders@biomet.com | |
Phone | 1-973-299-9300 |
btbs.csorders@biomet.com | |
Phone | 1-973-299-9300 |
btbs.csorders@biomet.com | |
Phone | 1-973-299-9300 |
btbs.csorders@biomet.com | |
Phone | 1-973-299-9300 |
btbs.csorders@biomet.com | |
Phone | 1-973-299-9300 |
btbs.csorders@biomet.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00888480588542 [Primary] |
MBP | Filler, Bone Void, Osteoinduction (W/O Human Growth Factor) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2015-10-19 |
00888480588542 | 20700421 |
00888480588535 | 20700321 |
00888480588528 | 20700221 |