| Primary Device ID | 00859193006326 |
| NIH Device Record Key | e3313391-8140-48f3-a1ad-18f43b3e1cd5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Philips ST SENSE NV 8 NeuroVascular Coil |
| Version Model Number | 4535-303-62942 |
| Company DUNS | 080151631 |
| Company Name | SCANMED, LLC |
| 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 | true |
| OTC Over-The-Counter | false |