| Primary Device ID | 07613327291384 |
| NIH Device Record Key | bf7755a3-f1b2-49b9-bbd1-1aa643967bd0 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 62-02321 |
| Catalog Number | 62-02321 |
| 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327291384 [Primary] |
| MQN | EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-09-23 |
| Device Publish Date | 2018-09-20 |
| 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 |