Finger response pad

GUDID 06430056480428

A finger response pad for detecting patient responses.

Megin Oy

Electroencephalograph

• Primary Device ID: 06430056480428
• NIH Device Record Key: 2ce5de85-7e60-46fc-a2ad-37ad5890b6e6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Finger response pad
• Version Model Number: NM20928X
• Company DUNS: 538025107
• Company Name: Megin Oy
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: false
• 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	06430056480428 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K091393

FDA Product Code

• OLY: Magnetoencephalograph

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: 2025-04-21
• Device Publish Date: 2025-04-11