| Primary Device ID | 08057432561588 |
| NIH Device Record Key | ebd923b9-d1d9-48a9-81b5-8b3882ae30f7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TFX / TRAUMAFIX |
| Version Model Number | TFX-20S62 |
| Company DUNS | 544150399 |
| Company Name | SINTEA PLUSTEK SRL |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| 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 |