| Primary Device ID | 03760177043091 |
| NIH Device Record Key | bd77d95b-64d6-4d45-87b6-95c44fc11088 |
| Commercial Distribution Discontinuation | 2022-06-02 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | HP+ |
| Version Model Number | T060422 |
| Catalog Number | T060422 |
| Company DUNS | 764746723 |
| Company Name | TEKNIMED |
| 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 | true |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |