| Primary Device ID | 03573026156930 | 
| NIH Device Record Key | 25386b28-baff-40b9-a68a-7f0458777ef4 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | VIDAS® LH | 
| Version Model Number | 30406-01 | 
| Company DUNS | 276816717 | 
| Company Name | BIOMERIEUX SA | 
| 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 | true | 
| 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 | 
| Storage Environment Temperature | Between 2 Degrees Celsius and 8 Degrees Celsius | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 03573026156930 [Primary] | 
| CEP | RADIOIMMUNOASSAY, LUTEINIZING HORMONE | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2019-11-13 | 
| Device Publish Date | 2019-11-05 | 
| 03573026631994 - ETEST® Aztreonam Avibactam (AZA) | 2025-10-03 ETEST is a quantitative technique for determining susceptibility of clinically significant bacteria. It provides a gradient of 1 | 
| 03573026633530 - ETEST® Imipenem Relebactam (IRPA) | 2025-07-01 ETEST is a quantitative technique for determining susceptibility of clinically significant bacteria. It provides a gradient of 1 | 
| 03573026559823 - THxID™ BRAF | 2025-06-09 Software used in combination with the THxIDTM- BRAF assay (used to identify patients with melanoma whose tumors harbor the BRAF | 
| 03573026637200 - VITEK® MS SOFTWARE v1.2 | 2025-05-07 The VITEK® MS Software is a computer application which supports the microbiology laboratory workflow for the VITEK® MS Systems | 
| 03573026626891 - VIDAS® TBI (GFAP, UCH-L1) | 2024-11-08 VIDAS TBI (GFAP, UCH-L1) is an automated quantitative test to be used on VIDAS3. It is intended to be used as an aid in the eval | 
| 03573026359096 - VITEK® MS-DS | 2024-04-30 The VITEK MS-DS target slides enable the identification of microorganisms according to the MALDI-TOF mass spectrometry method. | 
| 03573026359119 - VITEK® MS | 2024-04-29 MALDI-Tof Mass Spectrometry system used for microbial identification | 
| 03573026362843 - VITEK® MS FA | 2024-04-29 VITEK ® MS - FA is used to pretreat yeasts to facilitate their identification according to the MALDI - TOF method. It is used e | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  VIDAS  90812125  not registered Live/Pending | Compound Eye Inc. 2021-07-06 | 
|  VIDAS  86649688  4935355 Live/Registered | bioMérieux 2015-06-03 | 
|  VIDAS  79368562  not registered Live/Pending | ANGEL GEORGIEV LESOV 2023-03-09 | 
|  VIDAS  79368562  not registered Live/Pending | SVETLA ATANASOVA LESOVA 2023-03-09 | 
|  VIDAS  79171274  4916176 Live/Registered | bioMérieux 2015-05-28 | 
|  VIDAS  77640911  3849276 Live/Registered | bioMérieux 2008-12-29 | 
|  VIDAS  74072619  1785252 Live/Registered | VITEK SYSTEMS, INC. 1990-06-25 |