eego

GUDID B195ES220

eeg recording and review

eemagine Medical Imaging Solutions GmbH

Electroencephalographic monitoring system, stationary

• Primary Device ID: B195ES220
• NIH Device Record Key: f1a795c0-1d97-40d6-a92b-11f6c74332fa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: eego
• Version Model Number: ES-220
• Company DUNS: 313152485
• Company Name: eemagine Medical Imaging Solutions GmbH
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +493029048404
• Email: support@eemagine.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B195ES220 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K051825

FDA Product Code

• GWQ: Full-montage Standard Electroencephalograph

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: 2020-05-08
• Device Publish Date: 2020-04-30

On-Brand Devices [eego]

• B195LE200: eego component
• B195ES220: eeg recording and review