Primary Device ID | 10190302018999 |
NIH Device Record Key | 984cb090-fbdf-40f4-8f8d-90e973c0e96f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TaqPath™ COVID-19, Flu A, Flu B, RSV Select Positive Control |
Version Model Number | 963612 |
Company DUNS | 790376870 |
Company Name | LIFE TECHNOLOGIES CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10190302018999 [Primary] |
QOF | Multi-Target Respiratory Specimen Nucleic Acid Test Including Sars-Cov-2 And Other Microbial Agents |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-02-25 |
Device Publish Date | 2025-02-17 |
10190302019033 | Component 2 of 4 of A56124 (Applied Biosystems™ TaqPath™ COVID-19, Flu A, Flu B, RSV Select |
10190302018999 | Component 2 of 4 of A56123 (Applied Biosystems™ TaqPath™ COVID-19, Flu A, Flu B, RSV Select |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() TAQPATH 90979435 not registered Live/Pending |
Life Technologies Corporation 2020-11-16 |
![]() TAQPATH 90322432 not registered Live/Pending |
Life Technologies Corporation 2020-11-16 |
![]() TAQPATH 85846818 4530657 Live/Registered |
Life Technologies Corporation 2013-02-11 |