Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3021337381

FEI Number

3021337381

Entity Name

MUNEVO GMBH

City/State/Country

Munich Bavaria, DE

Establishment Address

Agnes-pockels-bogen 1, Munich Bavaria 80992, DE

Establishment Type(s)

Manufacture Medical Device,Complaint File Establishment per 21 CFR 820.198

Owner / Operator

Munevo GmBH (Owner Number: 10083888)

Owner / Operator Contact Address

Agnes-pockels-bogen 1, Munich, DE-BY 80992, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

munevo DRIVE

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KNN	Components, Wheelchair	Physical Medicine	Class 1	890.3920	2021-12-28

Official Correspondent

Michelle Halpain

US Agent Details

Robert Packard Business: Medical Device Academy Incorporated Email: rob@fdaestar.com Phone: (802) 2581881

Related Public Records

Same Entity

Munevo GmBH

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3021337381. Last updated year: 2026. Please use registration number 3021337381 when referencing this establishment in official correspondence.