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 |