Primary Device ID | 04049016151234 |
NIH Device Record Key | e7b70e1a-8fc3-4455-9e9e-3d060d02a3ba |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FITC-labelled anti-human IgG |
Version Model Number | AF 102-0540-R |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 |