| Primary Device ID | 09348215038847 |
| NIH Device Record Key | 3de7efcf-df0a-4d2b-903e-c3b24e9277f2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Trial Cups |
| Version Model Number | 112-152-193 |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| 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 | 09348215038847 [Primary] |
| HWT | Template |
| LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[09348215038847]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-06-18 |
| Device Publish Date | 2018-10-02 |
| 09348215038991 | 112-152-578 |
| 09348215038984 | 112-152-574 |
| 09348215038977 | 112-152-573 |
| 09348215038960 | 112-152-205 |
| 09348215038953 | 112-152-204 |
| 09348215038946 | 112-152-203 |
| 09348215038939 | 112-152-202 |
| 09348215038922 | 112-152-201 |
| 09348215038915 | 112-152-200 |
| 09348215038908 | 112-152-199 |
| 09348215038892 | 112-152-198 |
| 09348215038885 | 112-152-197 |
| 09348215038878 | 112-152-196 |
| 09348215038861 | 112-152-195 |
| 09348215038854 | 112-152-194 |
| 09348215038847 | 112-152-193 |
| 09348215038830 | 112-152-192 |
| 09348215038823 | 112-152-191 |