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EEGer4

by Eeg Software, LLC

EEGer4 is a Class II device made by Eeg Software, LLC, listed in FDA GUDID since 31 Aug 2016 (UDI-DI B258EEGER4), registry data as of 31 May 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 31 May 2026.

Regulatory status

as of registry sync 31 May 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB258EEGER4 UDI-DI Date31 Aug 2016ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name
Biofeedback system application software
Model / reference
4
Primary DI / UDI-DI
B258EEGER4
FDA product code
HCC
GMDN term
Biofeedback system application software
Device class
Class II
Regulation number
882.5050
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code HCC (Device, Biofeedback).

Other devices from Eeg Software, LLC

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)