Primary Device ID | 04049016096795 |
NIH Device Record Key | dfdbb3f8-a813-4877-835f-7584bf0a06dc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EUROStar III Plus |
Version Model Number | YG 0306-0101-3 |
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 | 04049016096795 [Primary] |
KEI | Condensers, Microscope |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-24 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EUROSTAR III PLUS 79249782 not registered Live/Pending |
EUROIMMUN Medizinische LabordiagnostikaAG 2018-11-20 |