| Primary Device ID | 07612334216663 |
| NIH Device Record Key | 4851c5f8-9ded-482e-92b2-62cff827ab3c |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 03.164.013 |
| Catalog Number | 03164013 |
| Company DUNS | 486711679 |
| Company Name | Synthes GmbH |
| Device Count | 1 |
| 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 | 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 |
| Phone | +1(800)255-2500 |
| xx@xx.xx |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07612334216663 [Direct Marking] |
| GS1 | 10886982311146 [Primary] |
| GDJ | CLAMP, SURGICAL, GENERAL & PLASTIC SURGERY |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07612334216663]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-12-07 |
| Device Publish Date | 2022-11-29 |
| 10886982350435 - NA | 2026-02-19 HALF BENNETT SMALL/LEFT |
| 10886982350442 - NA | 2026-02-19 HALF BENNETT SMALL/RIGHT |
| 10886982350459 - NA | 2026-02-19 HALF BENNETT LARGE/LEFT |
| 10886982350466 - NA | 2026-02-19 HALF BENNETT LARGE/RIGHT |
| 10886982351579 - NA | 2026-02-19 SHOULDER HOOK 2.2 MM TIP / 235 MM LENGTH |
| 10886982351661 - NA | 2026-02-19 T-HANDLE AO CONNECTOR |
| 10886982351678 - NA | 2026-02-19 T-HANDLE LARGE AO CONNECTOR |
| 10886982361288 - NA | 2026-02-19 5MM AWL, QC |