| Primary Device ID | E4947604741 |
| NIH Device Record Key | 4a50a794-a575-4f80-afd9-8abd7c4cd366 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Ceramil® Liquid |
| Version Model Number | Liquid CL 4 |
| Catalog Number | 760474 |
| Company DUNS | 300708950 |
| Company Name | Amann Girrbach AG |
| Device Count | 1 |
| DM Exempt | true |
| 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 | true |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | E4947604741 [Primary] |
| EIH | Powder, Porcelain |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-10-23 |
| Device Publish Date | 2020-10-15 |
| E4947616061 - Ceramill Sintron® | 2024-09-06 |
| E4947682281 - Zolid | 2023-03-17 |
| E4947682291 - Zolid | 2023-03-17 |
| E4947682301 - Zolid | 2023-03-17 |
| E4947682311 - Zolid | 2023-03-17 |
| E4947682321 - Zolid | 2023-03-17 |
| E4947682331 - Zolid | 2023-03-17 |
| E4947682371 - Zolid | 2023-03-17 |