Recording Cap G1 82-932

GUDID 08592566829321

82-932

DEYMED Diagnostic s.r.o.

Psychophysiological biofeedback system

• Primary Device ID: 08592566829321
• NIH Device Record Key: c5d4ece4-f429-4e40-b153-f3739ec96222
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Recording Cap G1
• Version Model Number: S (20“ - 21.5“)
• Catalog Number: 82-932
• 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	08592566829321 [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