| Primary Device ID | 09348215087173 |
| NIH Device Record Key | 86edfebc-cad8-4253-8f18-39276b49348a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Origin NS Stem |
| Version Model Number | 111-23-5001 |
| 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 | 09348215087173 [Primary] |
| MEH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-10-11 |
| Device Publish Date | 2021-10-01 |
| 09348215087289 | 111-23-5052 |
| 09348215087272 | 111-23-5051 |
| 09348215087265 | 111-23-5042 |
| 09348215087258 | 111-23-5041 |
| 09348215087241 | 111-23-5032 |
| 09348215087234 | 111-23-5031 |
| 09348215087227 | 111-23-5022 |
| 09348215087210 | 111-23-5021 |
| 09348215087203 | 111-23-5012 |
| 09348215087197 | 111-23-5011 |
| 09348215087180 | 111-23-5002 |
| 09348215087173 | 111-23-5001 |