Primary Device ID | 00627908080035 |
NIH Device Record Key | 434a341a-467c-4665-b818-2def0206fd80 |
Commercial Distribution Discontinuation | 2020-04-20 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Aurix Amplifier |
Version Model Number | 11003 |
Company DUNS | 201740425 |
Company Name | Vivosonic Inc |
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 | 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 |