Primary Device ID | 15391521420500 |
NIH Device Record Key | 06e72a9e-07a3-4819-9ded-a905f2cd1304 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TriniCLOT™ Imidazole Buffer |
Version Model Number | T1901 |
Company DUNS | 985039126 |
Company Name | TCOAG IRELAND LIMITED |
Device Count | 6 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 |
Storage Environment Temperature | Between 2 Degrees Celsius and 8 Degrees Celsius |
Storage Environment Temperature | Between 2 Degrees Celsius and 8 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05391521420503 [Unit of Use] |
GS1 | 15391521420500 [Primary] |
KQJ | System, Fibrinogen Determination |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-12 |
15391521421286 - TriniLIZE™ Stabilyte tubes | 2019-07-19 |
15391521420470 - TriniCLOT Lupus Screen | 2019-07-08 |
15391521420487 - TriniCLOT Lupus Confirm | 2019-07-08 |
15391521420630 - TriniCHECK Level 1 | 2019-07-08 |
15391521420647 - TriniCHECK Level 2 | 2019-07-08 |
15391521420654 - TriniCHECK Level 3 | 2019-07-08 |
15391521421309 - DT Wash | 2019-07-08 |
15391521421729 - DT Fluid | 2019-07-08 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TRINICLOT 77353758 3681953 Live/Registered |
TCOAG IRELAND LIMITED 2007-12-17 |