| Primary Device ID | 07640173161332 |
| NIH Device Record Key | a003aa53-7c83-4c20-b5f7-83d9c95c4fd7 |
| Commercial Distribution Discontinuation | 2019-08-07 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | VBR |
| Version Model Number | 2352 |
| Company DUNS | 482467792 |
| Company Name | coLigne 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |