| Primary Device ID | 08809970060005 |
| NIH Device Record Key | bbfde762-b77f-4224-8918-dea854c521a5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | EverEx Rehab |
| Version Model Number | 1.1.0 |
| Company DUNS | 695651100 |
| Company Name | EverEx |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | MR Safe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |