Primary Device ID | M3860250000501 |
NIH Device Record Key | 6ea27ecb-72de-4736-a22b-2137c7d8b77e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Accell Evo3 Putty |
Version Model Number | 02-5000-050 |
Catalog Number | 02-5000-050 |
Company DUNS | 801089152 |
Company Name | ISOTIS ORTHOBIOLOGICS, INC. |
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 | true |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)550-7155 |
irvine.customerservice@seaspin | |
Phone | +1(800)550-7155 |
irvine.customerservice@seaspin |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Storage Environment Temperature | Between 15 Degrees Celsius and 30 Degrees Celsius |
Storage Environment Temperature | Between 15 Degrees Celsius and 30 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10889981055400 [Primary] |
HIBCC | M3860250000501 [Secondary] |
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 | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-09-24 |
M3860250001001 | Accell Evo3 Putty, 10cc - demineralized human bone mixed with poloxamer resorbable reverse phas |
M3860250000501 | Accell Evo3 Putty,5 cc - demineralized human bone mixed with poloxamer resorbable reverse phase |
M3860250000251 | Accell Evo3 Putty, 2.5cc - demineralized human bone mixed with poloxamer resorbable reverse pha |