| Primary Device ID | 00813830024296 |
| NIH Device Record Key | 300c3d78-0dc2-4880-a7c1-1013f599ccf9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | International Digital Newport Flowmeter System |
| Version Model Number | 51000-INT |
| Catalog Number | 51000-INT |
| 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 |