Primary Device ID | 00856602005215 |
NIH Device Record Key | 17a82744-d898-42eb-a873-7f9d65d0e577 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Proteus Digital Health Feedback System |
Version Model Number | SPC-2329 |
Company DUNS | 149825791 |
Company Name | PROTEUS DIGITAL HEALTH, INC. |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |