| Primary Device ID | 34546540134555 |
| NIH Device Record Key | 95b84368-8ab3-4661-ba57-d413889bd3a0 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 01-02950 |
| Catalog Number | 01-02950 |
| Company DUNS | 316153956 |
| Company Name | Stryker Leibinger GmbH & Co. KG |
| Device Count | 12 |
| 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 | 14 Centimeter |
| Length | 14 Centimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04546540134554 [Unit of Use] |
| GS1 | 34546540134555 [Primary] |
| EHO | BAR, PREFORMED |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[34546540134555]
Moist Heat or Steam Sterilization
[34546540134555]
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 |
| 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 |