FUHRMANN GMBH

FDA Device Registration & Listing · Much North Rhine-Westphalia, DE · Registration 3013118873

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
3013118873
FEI Number
3013118873
Entity Name
FUHRMANN GMBH
City/State/Country
Much North Rhine-Westphalia, DE
Establishment Address
Boevingen 139, Much North Rhine-Westphalia 53804, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Fuhrmann GmbH (Owner Number: 10093039)
Owner / Operator Contact Address
Boevingen 139, Much, DE-NW 53804, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EPP Splint, Nasal Ear, Nose, Throat Class 1 874.5800 2025-04-22

Official Correspondent

Sara Abdul Karim

US Agent Details

Franz Menean Business: MEDAGENT Inc. Email: mail@medagent-usa.com Phone: (603) 5702039

Related Public Records

Same Entity

Fuhrmann 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 3013118873. Last updated year: 2026. Please use registration number 3013118873 when referencing this establishment in official correspondence.
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