Primary Device ID | 00813830023404 |
NIH Device Record Key | db0d68c2-8a2b-4e7f-844d-9b0c7e59ba73 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Digital Ultra Package C |
Version Model Number | 56200 |
Catalog Number | 56200 |
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 |