| Primary Device ID | 08800000912950 |
| NIH Device Record Key | e7bc853a-57c7-494e-b8da-a5a01738416b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | HU/HS/HG Prosthetic System |
| Version Model Number | HUSDA504R |
| Company DUNS | 689051793 |
| Company Name | Osstem Implant Co., Ltd. |
| 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 | true |
| Lot Batch | true |
| Serial Number | true |
| Manufacturing Date | true |
| 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 |