| Primary Device ID | 09348215054564 |
| NIH Device Record Key | f9c222b0-4bbe-49fe-9737-7b0f03d3b32c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Cemented Origin Stem |
| Version Model Number | 111-42-0802 |
| 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 | 09348215054564 [Primary] |
| LZO | Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-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 | 2020-08-17 |
| Device Publish Date | 2020-08-07 |
| 09348215054755 | 111-42-1803 |
| 09348215054748 | 111-42-1603 |
| 09348215054731 | 111-42-1503 |
| 09348215054724 | 111-42-1403 |
| 09348215054717 | 111-42-1303 |
| 09348215054700 | 111-42-1203 |
| 09348215054694 | 111-42-1103 |
| 09348215054687 | 111-42-1003 |
| 09348215054670 | 111-42-0903 |
| 09348215054663 | 111-42-0803 |
| 09348215054656 | 111-42-1802 |
| 09348215054649 | 111-42-1602 |
| 09348215054632 | 111-42-1502 |
| 09348215054625 | 111-42-1402 |
| 09348215054618 | 111-42-1302 |
| 09348215054601 | 111-42-1202 |
| 09348215054595 | 111-42-1102 |
| 09348215054588 | 111-42-1002 |
| 09348215054571 | 111-42-0902 |
| 09348215054564 | 111-42-0802 |