Splitter 63-906

GUDID 08592566639067

Neurofeedback device accessories

DEYMED Diagnostic s.r.o.

Psychophysiological biofeedback system

• Primary Device ID: 08592566639067
• NIH Device Record Key: 62bc7a23-8f6b-4d4a-a0ae-2cf3e00d6357
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Splitter
• Version Model Number: X-Connector: 2M - 2F
• Catalog Number: 63-906
• 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: true
• Serial Number: false
• 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	08592566639067 [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: 2023-06-20
• Device Publish Date: 2023-06-12

On-Brand Devices [Splitter]

• 08592566639067: Neurofeedback device accessories
• 08592566639050: Neurofeedback device accessories