| Primary Device ID | 09120073931344 |
| NIH Device Record Key | bba41f38-b6af-431b-9851-8e9e78ca7269 |
| Commercial Distribution Discontinuation | 2019-11-19 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Operator's Manual English USA |
| Version Model Number | V3.5.3 |
| Catalog Number | 21-FHZU-10002 |
| Company DUNS | 303562672 |
| Company Name | CNSystems Medizintechnik AG |
| 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 | false |
| Lot Batch | false |
| 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 | false |
| OTC Over-The-Counter | false |