| Primary Device ID | 00884883005952 |
| NIH Device Record Key | 9e9fdf51-d9fd-4814-870e-38097f53284c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DRI Oxycodone Calibrator 500 |
| Version Model Number | 100252 |
| Company DUNS | 122153799 |
| Company Name | Microgenics Corporation |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |