Primary Device ID | 04049016108740 |
NIH Device Record Key | 4eefa68e-b570-4365-ae0b-2b52dc8d52a4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EUROPLUS Granulocyte Mosaic 22 EUROPattern |
Version Model Number | FC 1201-1010-22 |
Company DUNS | 322209263 |
Company Name | EUROIMMUN Medizinische Labordiagnostika AG |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Storage Environment Temperature | Between 2 Degrees Celsius and 8 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04049016108740 [Primary] |
PIV | Automated Indirect Immunofluorescence Microscope And Software-Assisted System For Clinical Use |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2018-06-04 |
04049016135951 | FC 1201-18010-22 |
04049016135876 | FC 1201-2450-22 |
04049016135869 | FC 1201-12010-22 |
04049016135852 | FC 1201-1050-22 |
04049016108764 | FC 1201-2010-22 |
04049016108757 | FC 1201-2005-22 |
04049016108740 | FC 1201-1010-22 |
04049016108733 | FC 1201-1005-22 |