| Primary Device ID | 00082161082255 |
| NIH Device Record Key | d7a3fd1e-cb0a-4cc5-9ca2-f968fe3f4934 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NuRoo |
| Version Model Number | 08225 |
| Company DUNS | 091999771 |
| Company Name | BROWNMED, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | true |