| Primary Device ID | 07613252634416 |
| NIH Device Record Key | d65b0406-0e69-47c7-a403-bcc858c41614 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 62-01332 |
| Catalog Number | 62-01332 |
| 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 |
| Width | 30 Millimeter |
| Width | 30 Millimeter |
| Width | 30 Millimeter |
| Width | 30 Millimeter |
| Width | 30 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613252634416 [Primary] |
| MQN | EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07613252634416]
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 |
| 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 |