| Primary Device ID | 09348215088569 |
| NIH Device Record Key | 511e9eb7-63a9-4eea-9281-560db4523f8a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Origin DAA Stem, High Offset |
| Version Model Number | 111-39-1813 |
| Company DUNS | 751993028 |
| Company Name | SIGNATURE ORTHOPAEDICS PTY 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 | 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 | 09348215088569 [Primary] |
| LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-08-29 |
| Device Publish Date | 2022-08-19 |
| 09348215088569 | 111-39-1813 |
| 09348215088545 | 111-39-1613 |
| 09348215088521 | 111-39-1513 |
| 09348215088507 | 111-39-1413 |
| 09348215088484 | 111-39-1313 |
| 09348215088460 | 111-39-1213 |
| 09348215088446 | 111-39-1113 |
| 09348215088422 | 111-39-1013 |
| 09348215088408 | 111-39-0913 |
| 09348215088385 | 111-39-0813 |
| 09348215036454 | 111-39-1803 |
| 09348215036447 | 111-39-1603 |
| 09348215036430 | 111-39-1503 |
| 09348215036423 | 111-39-1403 |
| 09348215036416 | 111-39-1303 |
| 09348215036409 | 111-39-1203 |
| 09348215036393 | 111-39-1103 |
| 09348215036386 | 111-39-1003 |
| 09348215036379 | 111-39-0903 |
| 09348215036362 | 111-39-0803 |