| Primary Device ID | 09348215032548 |
| NIH Device Record Key | f9eea0db-ed25-4f68-9085-6ff249c2c6bb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Origin DAA Stem, Standard Offset |
| Version Model Number | 111-39-1502 |
| 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 | 09348215032548 [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 |
| 09348215088552 | 111-39-1812 |
| 09348215088538 | 111-39-1612 |
| 09348215088514 | 111-39-1512 |
| 09348215088491 | 111-39-1412 |
| 09348215088477 | 111-39-1312 |
| 09348215088453 | 111-39-1212 |
| 09348215088439 | 111-39-1112 |
| 09348215088415 | 111-39-1012 |
| 09348215088392 | 111-39-0912 |
| 09348215088378 | 111-39-0812 |
| 09348215032562 | 111-39-1802 |
| 09348215032555 | 111-39-1602 |
| 09348215032548 | 111-39-1502 |
| 09348215032531 | 111-39-1402 |
| 09348215032524 | 111-39-1302 |
| 09348215032517 | 111-39-1202 |
| 09348215032500 | 111-39-1102 |
| 09348215032494 | 111-39-1002 |
| 09348215032487 | 111-39-0902 |
| 09348215032470 | 111-39-0802 |