| Primary Device ID | 04049223104795 |
| NIH Device Record Key | a9f82a4e-6d23-4cbd-8aeb-98e2789d3c15 |
| Commercial Distribution Discontinuation | 2020-06-30 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Dummy, silver, type CCY |
| Version Model Number | AGD.A22 |
| Catalog Number | AGD.A22 |
| Company DUNS | 331080432 |
| Company Name | Eckert & Ziegler BEBIG GmbH |
| 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 | false |
| 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |