| Primary Device ID | 04049016109778 |
| NIH Device Record Key | de7572e4-6203-441f-9ae5-944845f07ea2 |
| Commercial Distribution Discontinuation | 2020-02-14 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | EUROLabLiquidHandler (30-08) |
| Version Model Number | YG 0830-0101-8 |
| Company DUNS | 322209263 |
| Company Name | EUROIMMUN Medizinische Labordiagnostika AG |
| 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 | 04049016109778 [Primary] |
| JQW | Station, Pipetting And Diluting, For Clinical Use |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2020-02-17 |
| Device Publish Date | 2016-09-24 |
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| 04049016159018 - UNIQO 160 | 2023-09-28 |
| 04049016152989 - IFA: Crithidia luciliae sensitive (anti-dsDNA) EUROPattern | 2023-07-13 |
| 04049016069355 - Adjustment solution | 2023-06-02 |
| 04049016151821 - Adjustment solution | 2023-06-02 |
| 04049016137740 - Free Testosterone ELISA | 2023-05-03 |
| 04049016140085 - Total Testosterone ELISA | 2023-05-03 |