| Primary Device ID | 00811403018789 |
| NIH Device Record Key | fa0112c5-45a9-4265-90b8-10356f768103 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Sodium Electrode |
| Version Model Number | AW-903393D |
| 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 |