| Primary Device ID | 03573026125752 |
| NIH Device Record Key | b0a6c328-a36b-41ed-88d7-c287cebca524 |
| Commercial Distribution Discontinuation | 2021-02-26 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | BacT/ALERT® Blood Collection Adapter Cap |
| Version Model Number | BacT/ALERT® Blood Collection Adapter Cap |
| Company DUNS | 086785110 |
| Company Name | BIOMERIEUX , INC. |
| Device Count | 120 |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03573026125752 [Package] Contains: 03573026556105 Package: [1 Units] Discontinued: 2021-02-26 Not in Commercial Distribution |
| GS1 | 03573026556099 [Unit of Use] |
| GS1 | 03573026556105 [Primary] |
| GIM | Tubes, Vacuum Sample, With Anticoagulant |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2021-03-23 |
| Device Publish Date | 2017-03-08 |
| 03573026145842 - VITEK®2 | 2025-06-09 VITEK®2 XL is an automated system that performs large volumes of bacterial ID & AST testings |
| 03573026553968 - VITEK®2 | 2025-06-09 VITEK ® 2 software 8.01 update, advanced software to run your VITEK ® 2 system |
| 03573026615499 - VITEK® COMPACT PRO | 2025-05-23 VITEK COMPACT PRO is an automated system that performs bacterial ID and AST. minimum, a total of 15 ID and/or AST cards can be |
| 03573026618285 - VITEK | 2025-05-23 Vitek 2 software V10 |
| 03573026641337 - VITEK® 2 AST-N815 | 2024-11-21 VITEK® 2 Gram Negative Susceptibility Card is intended for use with the VITEK 2 Systems to determine the susceptibility of clin |
| 00860007326905 - VITEK® REVEAL™ | 2024-10-17 The VITEK REVEAL Instrument is a benchtop instrument that processes up to four AST tests . Installation and operating details f |
| 00860007326912 - VITEK® REVEAL™ SEALER | 2024-10-17 The VITEK REVEAL SEALER provides the heat welding of the VITEK REVEAL SENSOR PANEL to the 96 well AST Drug Plate. |
| 03573026638900 - VITEK® REVEAL™ SENSOR PANEL | 2024-10-17 The VITEK REVEAL Reveal AST Assays are indicated for susceptibility testing of pathogenic bacteria |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() BACT/ALERT 77523447 3962173 Live/Registered |
bioMérieux, Inc. 2008-07-16 |
![]() BACT/ALERT 75022103 2017525 Live/Registered |
BIOMERIEUX, INC. 1995-11-20 |