| Primary Device ID | 03760357975075 |
| NIH Device Record Key | 4de0f876-3006-4dd2-97a9-1f8aca3c598a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NICRALLIUM N4 |
| Version Model Number | Powder 16 µm |
| Company DUNS | 346973803 |
| Company Name | BERNARD CERVOS SOCIETE |
| 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 | 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 |