| Primary Device ID | 08033315120394 |
| NIH Device Record Key | 4d0eca75-1570-4527-b74b-4f58f13df649 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BIONEN |
| Version Model Number | 0210100 |
| Company DUNS | 444022750 |
| Company Name | BIONEN SAS DI BARBARA NENCIONI & C. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | 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 |