| Primary Device ID | 09348215122072 |
| NIH Device Record Key | f3b0bd69-dcde-448f-bcad-9c102140d69f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Bio-composite Screw |
| Version Model Number | 121-05-6238 |
| Company DUNS | 751993028 |
| Company Name | SIGNATURE ORTHOPAEDICS PTY LTD |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 09348215122072 [Primary] |
| HWC | Screw, Fixation, Bone |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-08-14 |
| Device Publish Date | 2023-08-04 |
| 09348215116705 | 121-05-2379 |
| 09348215116699 | 121-05-2329 |
| 09348215116682 | 121-05-1379 |
| 09348215116675 | 121-05-1329 |
| 09348215116668 | 121-05-0379 |
| 09348215116651 | 121-05-0329 |
| 09348215116644 | 121-05-9379 |
| 09348215116637 | 121-05-9329 |
| 09348215116620 | 121-05-9278 |
| 09348215116613 | 121-05-9279 |
| 09348215116606 | 121-05-8329 |
| 09348215116590 | 121-05-8278 |
| 09348215116583 | 121-05-8279 |
| 09348215029135 | 121-05-8238 |
| 09348215029128 | 121-05-8239 |
| 09348215029111 | 121-05-7329 |
| 09348215029104 | 121-05-7278 |
| 09348215122119 | 121-05-7279 |
| 09348215122102 | 121-05-7238 |
| 09348215122096 | 121-05-7239 |
| 09348215122089 | 121-05-6279 |
| 09348215122072 | 121-05-6238 |
| 09348215122065 | 121-05-6239 |
| 09348215122058 | 121-05-5239 |