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 |