| Primary Device ID | 08056600520532 |
| NIH Device Record Key | f80c5f6b-2ea8-4ac1-9154-9956e699ee37 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | N23 CCD System |
| Version Model Number | N23 |
| Catalog Number | N2360RHR1 |
| Company DUNS | 435743877 |
| Company Name | NICAL SPA |
| 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 | true |
| Serial Number | true |
| Manufacturing Date | true |
| 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 |