| Primary Device ID | 10603295033004 |
| NIH Device Record Key | e02e5aae-0a44-45b0-9cf0-19805ce1e01e |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 1365-07-000 |
| Catalog Number | 136507000 |
| Company DUNS | 989365556 |
| Company Name | DEPUY (IRELAND) |
| 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 | false |
| 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 |
| Phone | +1(800)255-2500 |
| xx@xx.xx |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10603295033004 [Primary] |
| LPH | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-04-06 |
| Device Publish Date | 2015-09-24 |
| 10603295509202 - DEPUY SYNTHES | 2024-04-09 DEPUY SYNTHES 28 MM +1.5 TRIAL HEAD |
| 10603295509219 - DEPUY SYNTHES | 2024-04-09 DEPUY SYNTHES 28 MM +5 TRIAL HEAD |
| 10603295509226 - DEPUY SYNTHES | 2024-04-09 DEPUY SYNTHES 28 MM +8.5 TRIAL HEAD |
| 10603295509233 - DEPUY SYNTHES | 2024-04-09 DEPUY SYNTHES 32 MM +1 TRIAL HEAD |
| 10603295509240 - DEPUY SYNTHES | 2024-04-09 DEPUY SYNTHES 32 MM +5 TRIAL HEAD |
| 10603295509257 - DEPUY SYNTHES | 2024-04-09 DEPUY SYNTHES 32 MM +9 TRIAL HEAD |
| 10603295509264 - DEPUY SYNTHES | 2024-04-09 DEPUY SYNTHES 32 MM +13 TRIAL HEAD |
| 10603295509288 - DEPUY SYNTHES | 2024-04-09 DEPUY SYNTHES 36 MM +1.5 TRIAL HEAD |