| Primary Device ID | 00860011334606 |
| NIH Device Record Key | 1f4c2c5a-783d-4bfe-8800-8ef0211b4b3e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ddR Cruze |
| Version Model Number | ddR Cruze |
| Company DUNS | 482051190 |
| Company Name | Swissray Medical 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 | true |
| 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 |