Primary Device ID | M386563000501 |
NIH Device Record Key | 77d16fd3-40a2-49e1-b729-52cd6ca9363c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | OsteoSurge 100 Putty |
Version Model Number | 56300050 |
Catalog Number | 56300050 |
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 | 10889981055813 [Primary] |
HIBCC | M386563000501 [Secondary] |
MQV | FILLER, BONE VOID, CALCIUM COMPOUND |
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 |
M386563001001 | OsteoSurge100, 10cc - demineralized human bone mixed with poloxamer reverse phase medium. OsteoS |
M386563000501 | OsteoSurge100, 5cc - demineralized human bone mixed with poloxamer reverse phase medium. OsteoSu |
M386563000251 | OsteoSurge100, 2.5cc - demineralized human bone mixed with poloxamer reverse phase medium. Osteo |
M386563000101 | OsteoSurge100, 1cc - demineralized human bone mixed with poloxamer reverse phase medium. OsteoSu |