| Primary Device ID | 00861714000355 |
| NIH Device Record Key | 9f8597fd-b41a-4749-ab7e-2cd3bfc0e05d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Cerebrotech Fluids Monitor |
| Version Model Number | 5000 |
| Company DUNS | 048219350 |
| Company Name | CEREBROTECH MEDICAL SYSTEMS INC |
| 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 | 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 | true |
| OTC Over-The-Counter | false |