| Primary Device ID | 08033891328856 |
| NIH Device Record Key | 5de26791-25c9-44c7-a97f-a300d4f339ec |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CHORUS TRIO |
| Version Model Number | 81200 |
| Catalog Number | 81200 |
| Company DUNS | 435036669 |
| Company Name | DIESSE DIAGNOSTICA SENESE SPA |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08033891328856 [Primary] |
| JJE | Analyzer, Chemistry (Photometric, Discrete), For Clinical Use |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-12-22 |
| Device Publish Date | 2023-12-14 |
| 08033891320010 - CHORUS ECHINOCOCCUS IgG | 2024-01-30 |
| 08033891320522 - VACU-TEC | 2024-01-30 |
| 08033891320645 - VACU-TEC CUVETTE-L | 2024-01-30 |
| 08033891320690 - VES-TEC CUVETTE-L | 2024-01-30 |
| 08033891321086 - VACU-TEC S.C. | 2024-01-30 |
| 08033891321093 - VACU-TEC S.C. STERILE | 2024-01-30 |
| 08033891322083 - CHORUS Q FEVER PHASE II IgG | 2024-01-30 |
| 08033891322434 - CHORUS MEASLES IgG | 2024-01-30 |