| Primary Device ID | 00190707005191 |
| NIH Device Record Key | 072fa0b8-cae2-43d0-bcab-1f9d6c5ef976 |
| Commercial Distribution Discontinuation | 2019-01-25 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Tru-Flavor |
| Version Model Number | 600-006 |
| Company DUNS | 062165188 |
| Company Name | ORTHO ORGANIZERS, 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 | 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 | true |
| OTC Over-The-Counter | false |