Primary Device ID | 08592566419003 |
NIH Device Record Key | afa453af-f2f7-48c9-b088-f4285b88ed4a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TruScan Neurofeedback Adapter |
Version Model Number | 41-900 |
Catalog Number | 41-900 |
Company DUNS | 495566056 |
Company Name | DEYMED Diagnostic s.r.o. |
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 | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08592566419003 [Primary] |
HCC | Device, Biofeedback |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-11-03 |
Device Publish Date | 2023-10-26 |
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