| Primary Device ID | 04049016109761 |
| NIH Device Record Key | 1cc925d9-6c71-4949-99e4-5d811545eabc |
| Commercial Distribution Discontinuation | 2020-02-14 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | EUROLabLiquidHandler (30-05) |
| Version Model Number | YG 0830-0101-5 |
| 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 |