| Primary Device ID | 07615208291551 |
| NIH Device Record Key | 6505b99c-0fab-49bb-8df9-84f3b53d1e05 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Cervitec F |
| Version Model Number | 745815AL |
| Catalog Number | 745815AL |
| Company DUNS | 448015938 |
| Company Name | IVOCLAR VIVADENT AKTIENGESELLSCHAFT |
| 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 |