| Primary Device ID | 07613252634379 |
| NIH Device Record Key | 1ada2250-8e5f-473f-ba44-e9cda7d3962a |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 62-01323 |
| Catalog Number | 62-01323 |
| 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 | true |
| 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 | 20 Millimeter |
| Length | 20 Millimeter |
| Length | 20 Millimeter |
| Length | 20 Millimeter |
| Length | 20 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613252634379 [Primary] |
| MQN | EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07613252634379]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-09-23 |
| Device Publish Date | 2015-09-24 |
| 07613327300024 - NA | 2024-04-18 |
| 07613327556285 - NA | 2024-02-27 Facial iD MF 1 Mesh |
| 07613327556308 - NA | 2024-02-23 Facial iD MF 2 meshes |
| 07613327556322 - NA | 2024-02-23 Facial iD MF 3 meshes |
| 07613327556346 - NA | 2024-02-23 Facial iD MF 4 meshes |
| 07613327556377 - NA | 2024-02-23 Facial iD MF 5 meshes |
| 07613327556391 - NA | 2024-02-23 Facial iD MF 6 meshes |
| 07613327556827 - NA | 2024-02-23 Facial iD MF 1 mesh kit |