| Primary Device ID | 00817770020868 |
| NIH Device Record Key | c59f73e8-97e1-4cad-9b32-56528b5c8635 |
| Commercial Distribution Discontinuation | 2019-05-06 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Handi+ |
| Version Model Number | R218P12-005 |
| 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 |