Recording Cap G1 82-934

GUDID 08592566829345

82-934

DEYMED Diagnostic s.r.o.

Psychophysiological biofeedback system

• Primary Device ID: 08592566829345
• NIH Device Record Key: d50ffeec-6084-4ea1-8491-de09d1dc363e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Recording Cap G1
• Version Model Number: L (23“ - 25“)
• Catalog Number: 82-934
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	08592566829345 [Primary]

FDA Product Code

• HCC: Device, Biofeedback

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-11-03
• Device Publish Date: 2023-10-26

On-Brand Devices [Recording Cap G1]

• 08592566629341: Neurofeedback device accessories
• 08592566629334: Neurofeedback device accessories
• 08592566629327: Neurofeedback device accessories
• 08592566629310: Neurofeedback device accessories
• 08592566829345: 82-934
• 08592566829338: 82-933
• 08592566829321: 82-932
• 08592566829314: 82-931