| Primary Device ID | 00742860000065 |
| NIH Device Record Key | a740cd9c-fbbb-4e8b-bc58-23340106ee02 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | OSOM Flu SARS-CoV-2 Combo Test |
| Version Model Number | 1080 |
| Company DUNS | 966812344 |
| Company Name | SEKISUI DIAGNOSTICS, LLC |
| Device Count | 27 |
| 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 | 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 | 00742860000065 [Primary] |
| GS1 | 10742860000062 [Unit of Use] |
| GS1 | 50742860100661 [Package] Package: [1 Units] Discontinued: 2025-12-12 Not in Commercial Distribution |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2025-12-23 |
| Device Publish Date | 2024-12-16 |
| 00742860000065 - OSOM Flu SARS-CoV-2 Combo Test | 2025-12-23OSOM Flu SARS-CoV-2 Combo Test |
| 00742860000065 - OSOM Flu SARS-CoV-2 Combo Test | 2025-12-23 OSOM Flu SARS-CoV-2 Combo Test |
| 10742860100663 - OSOM RSV Test Home | 2025-05-27 OSOM RSV Test |
| 00628063401291 - Acetaminophen | 2023-05-16 |
| 00628063401307 - Acetaminophen Calibrator | 2023-05-16 |
| 00628063401314 - Alinity c Acetaminophen | 2023-05-16 |
| 00628063401321 - Alinity c Acetaminophen Calibrator | 2023-05-16 |
| 10742860100397 - OSOM ULTRA PLUS FLU A&B Test | 2022-06-10 |
| 00628063401222 - DC-TROL LEVELS 1 & 2 | 2020-04-07 |