| Primary Device ID | 00817770020264 |
| NIH Device Record Key | 658c24d8-a483-4000-8f53-59a0751789b5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MAX-80i |
| Version Model Number | R113P11 |
| Company DUNS | 169911828 |
| Company Name | MAXTEC, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | 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 |