BEE MEDIC GMBH

FDA Device Registration & Listing · Bamberg Bavaria, DE · Registration 3038189172

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3038189172
FEI Number
3038189172
Entity Name
BEE MEDIC GMBH
City/State/Country
Bamberg Bavaria, DE
Establishment Address
Kirschaeckerstr. 25, Bamberg Bavaria 96052, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
BEE Medic GmbH (Owner Number: 10093168)
Owner / Operator Contact Address
Kirschaeckerstr. 25, Bamberg, DE-BY 96052, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K073557
PMA Number
N/A

All Registered Proprietary Names

HBI Database HBIdb NeuroAmp EEG NeuroAmp

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OLU Normalizing Quantitative Electroencephalograph Software Neurology Class 2 882.1400 2025-04-10
HCC Device, Biofeedback Neurology Class 2 882.5050 2025-04-10

Official Correspondent

Bernhard Wandernoth

US Agent Details

Bernhard Wandernoth Business: BEE Systems, Inc Email: prrc@bee.systems Phone: (818) 6481773

Related Public Records

Same Entity

BEE Medic GmbH
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K873418 Bodylog, Inc. BODYLOG STRESS REDUCTION PACKAGE 1987-12-17
K792659 Bio-Feedback Systems, Inc. FEEDBACK EDR SYSTEM MODEL ME-1 1980-01-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3038189172. Last updated year: 2026. Please use registration number 3038189172 when referencing this establishment in official correspondence.
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