| Primary Device ID | 07613327122879 |
| NIH Device Record Key | 589aa9d9-9375-48dc-92dc-dad600e5edb2 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 01-01036 |
| Catalog Number | 01-01036 |
| Company DUNS | 316153956 |
| Company Name | Stryker Leibinger GmbH & Co. KG |
| 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 | true |
| 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 | 19 Centimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327122879 [Primary] |
| GWO | Plate, cranioplasty, preformed, alterable |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07613327122879]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2017-03-31 |
| 07613327353563 - NA | 2025-02-27 NAVIGATED DRILL GUIDE SET CONTAINER |
| 07613252196259 - FLUOROMAP | 2025-02-05 FLUOROMAP 1.0 - SALES DEMO CD |
| 07613252286578 - FLUOROMAP | 2025-02-05 FLUOROMAP 1.0 SOFTWARE |
| 07613252286622 - FLUOROMAP | 2025-02-05 FLUOROMAP 1.0 - ENABLE |
| 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 |