| Primary Device ID | M578YO3IVD2 |
| NIH Device Record Key | f343d572-0ff2-437e-a1c8-941c0da980ac |
| Commercial Distribution Discontinuation | 2024-07-25 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Sensititre |
| Version Model Number | YO3IVD |
| Company DUNS | 298203498 |
| Company Name | TREK DIAGNOSTIC SYSTEMS LIMITED |
| Device Count | 10 |
| 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 | true |
| 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 | false |
| OTC Over-The-Counter | false |
| Phone | 8006427029 |
| info.Trek.US@thermofisher.com | |
| Phone | 8006427029 |
| info.Trek.US@thermofisher.com | |
| Phone | 8006427029 |
| info.Trek.US@thermofisher.com | |
| Phone | 8006427029 |
| info.Trek.US@thermofisher.com | |
| Phone | 8006427029 |
| info.Trek.US@thermofisher.com | |
| Phone | 8006427029 |
| info.Trek.US@thermofisher.com | |
| Phone | 8006427029 |
| info.Trek.US@thermofisher.com | |
| Phone | 8006427029 |
| info.Trek.US@thermofisher.com | |
| Phone | 8006427029 |
| info.Trek.US@thermofisher.com | |
| Phone | 8006427029 |
| info.Trek.US@thermofisher.com | |
| Phone | 8006427029 |
| info.Trek.US@thermofisher.com | |
| Phone | 8006427029 |
| info.Trek.US@thermofisher.com | |
| Phone | 8006427029 |
| info.Trek.US@thermofisher.com | |
| Phone | 8006427029 |
| info.Trek.US@thermofisher.com | |
| Phone | 8006427029 |
| info.Trek.US@thermofisher.com | |
| Phone | 8006427029 |
| info.Trek.US@thermofisher.com | |
| Phone | 8006427029 |
| info.Trek.US@thermofisher.com |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | M578YO3IVD0 [Unit of Use] |
| HIBCC | M578YO3IVD2 [Primary] |
| NGZ | Susceptibility Test Plate, Antifungal |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2024-07-26 |
| Device Publish Date | 2016-09-24 |
| 05032384571819 | OMADFAST |
| M578FDANDSF2 | FDANDSF |
| M578ESB1F2 | ESB1F |
| M578YO3IVD2 | YO3IVD |
| M578YO2IVD2 | YO2IVD |
| 05032384548606 | CMT1DSTF |
| 05032384575466 | CMC1OUNF |
| 05032384569151 | CMC1AXPF |
| 05032384569120 | CMC6VGNF |
| 05032384511419 | CMC1YOGV |
| 05032384505913 | CMC1GNCC |
| 05032384571321 | YO4IVD |
| 05032384529247 | MDRGN2F |
| 05032384501311 | FDANDSF |
| 05032384497546 | CMC5MDOH |
| 05032384474288 | ESB1F |
| 05032384571635 | CMC1OUPF |
| 05032384571628 | MDRGN4F |
| 05032384571697 | CMC1MDNF |
| 05032384571703 | GNUR5F |
| 05032384571727 | MDRGN3F |
| 05032384571710 | STP7F |
| 05032384575459 | CMT1DGPF |
| 05032384544554 | CMC1GPVF |
| 05032384571734 | CMC5VGPF |
| 05032384571796 | CMC4VGPF |
| 05032384571666 | CMC5VGNF |
| 05032384571802 | CMC9ARUP |
| 05032384571772 | MEROVAB |
| 05032384571505 | CMC3VGPF |
| 05032384474561 | YO2IVD |
| 05032384503513 | YO3IVD |
| 05032384571659 | CMC1GPUF |
| 05032384571680 | CMC7AFLF |
| 05032384571673 | CMC6AFLF |
| M578STP6F2 | STP6F |
| M578NF2 | NF |
| M578GPALL1F2 | GPALL1F |
| M578GNUR3F2 | GNUR3F |
| M578GN4F2 | GN4F |
| M578GN3F2 | GN3F |
| M578GN2F2 | GN2F |
| 05032384580613 | ARUP1MDF |
| 05032384580132 | HPB2 |
| 05032384571758 | GN7F |
| 05032384571574 | FDANDPF |
| 05032384571482 | GPALL3F |
| 05032384571499 | GPN3F |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SENSITITRE 73161811 1126962 Dead/Cancelled |
UAC INTERNATIONAL LIMITED 1978-03-13 |
![]() SENSITITRE 73099700 1113936 Live/Registered |
UAC INTERNATIONAL LIMITED 1976-09-13 |