Primary Device ID | 10889981149369 |
NIH Device Record Key | 2222623b-a573-463f-aafc-69582fb5d9e2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | OsteoBallast |
Version Model Number | 56800115 |
Catalog Number | 56800115 |
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 25 Degrees Celsius |
Storage Environment Temperature | Between 15 Degrees Celsius and 25 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10889981149369 [Primary] |
MBP | Filler, bone void, osteoinduction (w/o human growth factor) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2018-04-05 |
10889981149376 | OsteoBallast, 85x17.5mm |
10889981149369 | OsteoBallast, 85x11mm |
10889981149352 | OsteoBallast, 45x17.5mm |
10889981149345 | OsteoBallast, 45x11mm |
10889981232153 | OsteoBallast®, 150x11mm, 2-pack |
10889981232146 | OsteoBallast®, 150x11mm, 1-pack |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
OSTEOBALLAST 87584010 5728747 Live/Registered |
IsoTis OrthoBiologics, Inc. 2017-08-25 |