| Primary Device ID | 00885797692214 |
| NIH Device Record Key | 7d179d46-6607-486f-ab6d-c219671b777f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Mini Twin |
| Version Model Number | KM13552 |
| Company DUNS | 007058183 |
| Company Name | Rmo, 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 | true |
| Lot Batch | true |
| Serial Number | false |
| 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 |