Primary Device ID | 05711781001678 |
NIH Device Record Key | 68aa85a9-31d3-4b28-a95c-ce8b5096eea8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Amplitude By Auditdata |
Version Model Number | Amplitude T4 |
Company DUNS | 310385849 |
Company Name | Auditdata A/S |
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 |