| Primary Device ID | 08800049453230 |
| NIH Device Record Key | 4e3c6493-cd53-47d8-b483-8ad9e3d3e58e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | UFIII Fixture |
| Version Model Number | UFIII 4015S |
| Company DUNS | 631085206 |
| Company Name | DIO Corporation |
| 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 | true |
| Lot Batch | true |
| Serial Number | true |
| Manufacturing Date | true |
| 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 |