Primary Device ID | 00813830028317 |
NIH Device Record Key | 80a06c61-2be9-43c5-88d3-96120b6d0791 |
Commercial Distribution Discontinuation | 2099-02-22 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Digital Ultra, Package E, UK |
Version Model Number | 56400-UK |
Catalog Number | 56400-UK |
Company DUNS | 088302096 |
Company Name | ACCUTRON, 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 | true |
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 | true |
OTC Over-The-Counter | false |