| Primary Device ID | 04260759930058 |
| NIH Device Record Key | 76411c65-e6f9-49d1-b491-691e9a887c30 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RIWOtrack Cube4D |
| Version Model Number | E011106-4K/8 RW |
| Catalog Number | E011106-4K/8 RW |
| Company DUNS | 312623008 |
| Company Name | Fiagon GmbH |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| 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 |