| Primary Device ID | H9810460002902S0 |
| NIH Device Record Key | 9db15a45-4976-4571-9e80-75b14c7817ca |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 04.600.029.02S |
| Catalog Number | 0460002902S |
| Company DUNS | 486711679 |
| Company Name | Synthes GmbH |
| Device Count | 2 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | 20705034734214 [Primary] |
| GS1 | 80705034734216 [Unit of Use] |
| HIBCC | H9810460002902S0 [Secondary] |
| HXW | BENDER |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2025-12-11 |
| Device Publish Date | 2019-08-20 |
| H9810460002902S0 - NA | 2025-12-11TI DISTRACTOR PINS-16MM STERILE |
| H9810460002902S0 - NA | 2025-12-11 TI DISTRACTOR PINS-16MM STERILE |
| H9810460002910S0 - NA | 2025-12-11 TI DISTRACTOR PINS-16MM STERILE |
| 07612334270139 - EXPert Nail | 2025-10-02 TRAY F/TIBIAL NAIL EX SP INSTR |
| H679310930 - NA | 2025-10-01 SMALL CHUCK WITH KEY |
| 10886982350190 - NA | 2025-09-22 2.0MM STRAIGHT PLATE 20 HOLES |
| 10887587078465 - NA | 2025-09-19 NONRETAINING SCREWDRIVER BLADE FOR 90DEG SCREWDRIVER |
| 10886982349873 - NA | 2025-09-01 CANNULATED CIRCULAR REAMER 16MM |
| 10886982349880 - NA | 2025-09-01 CANNULATED CIRCULAR REAMER 18MM |