Primary Device ID | 00811403017058 |
NIH Device Record Key | c2b6dc8c-2673-40aa-b48d-c3b26624ae7a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sodium Electrode |
Version Model Number | OY-MU9194D |
Company DUNS | 947514303 |
Company Name | Diamond Diagnostics Inc. |
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 | true |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |