| Primary Device ID | 00817365020204 |
| NIH Device Record Key | 058b942e-6d90-438b-b9e4-d31c22b1d2dd |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Fusion1K |
| Version Model Number | FUS1K80CA |
| Company DUNS | 958807575 |
| Company Name | MOXI ENTERPRISES, LLC |
| 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 | 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 | false |
| OTC Over-The-Counter | false |