FDA UDI In Commercial Distribution 🇺🇸 United States

eego

DI: B195ES220 · Model: ES-220 · eemagine Medical Imaging Solutions GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
eego
Primary DI
B195ES220
Version / Model
ES-220
Company Name
eemagine Medical Imaging Solutions GmbH
Labeler DUNS
313152485
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-30
Public Version
2
Public Version Date
2025-09-30
Public Version Status
Update
Public Device Record Key
f1a795c0-1d97-40d6-a92b-11f6c74332fa

Device Description

eeg recording and review

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GWQ Full-montage Standard Electroencephalograph

GMDN Terms

Code Name
38736 Electroencephalographic monitoring system

Identifiers

Type ID
Primary B195ES220

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K051825 000