| Primary Device ID | 09348215038274 |
| NIH Device Record Key | c1fc700f-8dfe-4bbf-9d52-c4cec74b3311 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Trial Head |
| Version Model Number | 112-182-040 |
| 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 | 09348215038274 [Primary] |
| HWT | Template |
| LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[09348215038274]
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 |
| 09348215038410 | 112-182-046 |
| 09348215038403 | 112-182-045 |
| 09348215038397 | 112-182-044 |
| 09348215038380 | 112-182-043 |
| 09348215038373 | 112-182-024 |
| 09348215038366 | 112-182-023 |
| 09348215038359 | 112-182-022 |
| 09348215038342 | 112-182-021 |
| 09348215038335 | 112-182-020 |
| 09348215038328 | 112-182-019 |
| 09348215038311 | 112-182-018 |
| 09348215038304 | 112-182-017 |
| 09348215038298 | 112-182-042 |
| 09348215038281 | 112-182-041 |
| 09348215038274 | 112-182-040 |