| Primary Device ID | 37613153154274 |
| NIH Device Record Key | eabf72f1-ee49-40d8-aba7-472ae091b837 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 01-02940 |
| Catalog Number | 01-02940 |
| Company DUNS | 316153956 |
| Company Name | Stryker Leibinger GmbH & Co. KG |
| Device Count | 10 |
| 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Length | 11.5 Centimeter |
| Length | 11.5 Centimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613153154273 [Unit of Use] |
| GS1 | 37613153154274 [Primary] |
| EHO | BAR, PREFORMED |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[37613153154274]
Moist Heat or Steam Sterilization
[37613153154274]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2017-01-11 |
| 07613327401523 - NA | 2025-01-17 SternalPlate, Transverse, w/ bars |
| 07613327401554 - NA | 2025-01-17 SternalPlate, T |
| 07613327401561 - NA | 2025-01-17 SternalPlate, Transverse, w/ bars |
| 07613327401738 - NA | 2025-01-17 SternalPlate, T |
| 07613327634952 - NA | 2024-12-16 Drill for 6514-7-200 WL 16mm |
| 07613327634969 - NA | 2024-12-16 Drill for 6514-7-200 WL 12mm |
| 07613327634976 - NA | 2024-12-16 Drill for 6514-7-200 WL 10mm |
| 07613327634983 - NA | 2024-12-16 Drill for 6514-7-200 WL 12mm |