Skip to content

BE Micro Recorder B9700073000

by Eb Neuro SpA

BE Micro Recorder B9700073000 is a Class II device made by Eb Neuro SpA, listed in FDA GUDID since 2 Apr 2019 (UDI-DI 08056446900017), registry data as of 23 Oct 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08056446900017 UDI-DI Date2 Apr 2019ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
BE Micro Recorder
Generic name
Electroencephalographic ambulatory recorder
Model / reference
B9700073000
Primary DI / UDI-DI
08056446900017
FDA product code
GWQ, GWL, OLV, MNR
GMDN term
Electroencephalographic ambulatory recorder
Device class
Class II
Regulation number
882.1400, 882.1835, 868.2375
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code GWQ (Full-Montage Standard Electroencephalograph).

Other devices from Eb Neuro SpA

See all devices from Eb Neuro SpA →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)