| Primary Device ID | 07640187462210 |
| NIH Device Record Key | 3c45777a-1a83-4dc7-9b8e-0927d1f3e728 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | 1.8mm K-Wire Tube |
| Version Model Number | B-420025 |
| Company DUNS | 480244832 |
| Company Name | Bonebridge AG |
| 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 | 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 | true |
| OTC Over-The-Counter | false |