FlexiCAP 82-915

GUDID 08592566829154

Psychophysiological biofeedback system

Primary Device ID	08592566829154
NIH Device Record Key	670ce2d9-844f-4cbf-8b3d-8caa5cf41631
Commercial Distribution Status	In Commercial Distribution
Brand Name	FlexiCAP
Version Model Number	Size S 51-55 cm, 20-21,5 in
Catalog Number	82-915
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	08592566829154 [Primary]

HCC	Device, Biofeedback

Steralize Prior To Use	false
Device Is Sterile	false

08592566629174	Neurofeedback device accessories
08592566629167	Neurofeedback device accessories
08592566629150	Neurofeedback device accessories
08592566629143	Neurofeedback device accessories
08592566629136	Neurofeedback device accessories
08592566629129	Neurofeedback device accessories
08592566629112	Neurofeedback device accessories
08592566629105	Neurofeedback device accessories
08592566829178	Size L 59-63 cm, 23-25 in
08592566829161	Size M 55-59 cm, 21,5-23 in
08592566829154	Size S 51-55 cm, 20-21,5 in
08592566829147	Size XS 47-51 cm, 18,5-20 in
08592566829130	82-913
08592566829123	82-912
08592566829116	82-911
08592566829109	82-910

Mark Image Registration \| Serial	Company Trademark Application Date
FLEXICAP 85736631 4541531 Live/Registered	Syfer Technology Limited 2012-09-24
FLEXICAP 74292696 1822802 Dead/Cancelled	139001 CANADA INC. 1992-07-08