Primary Device ID | 04049016109754 |
NIH Device Record Key | d0b87f3a-cfe9-44ac-b7e7-edf5da001e0f |
Commercial Distribution Discontinuation | 2020-02-14 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | EUROLabLiquidHandler (30-10) |
Version Model Number | YG 0830-0101-10 |
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 | 04049016109754 [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 |
04049016151999 - Mounting medium (IFA) | 2024-07-25 |
04049016144595 - IFA: Oesophagus (Monkey) IgA EUROPattern | 2024-05-27 |
04049016125228 - EUROArrayScanner | 2023-11-28 |
04049016159704 - EUROPLUS Granulocyte Mosaic 32 | 2023-10-13 |
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 |