| Primary Device ID | 00813830026832 |
| NIH Device Record Key | 0289e48c-b45d-4f0c-8557-3c6f4e9987ec |
| Commercial Distribution Discontinuation | 2199-04-18 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Ultra PC % Flowmeter, EU Model-50 % N2O |
| Version Model Number | 31975-EU50 |
| Catalog Number | 31975-EU50 |
| Company DUNS | 088302096 |
| Company Name | ACCUTRON, INC. |
| Device Count | 1 |
| DM Exempt | true |
| 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 | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |