MEDIFA GMBH

FDA Device Registration & Listing · Finnentrop North Rhine-Westphalia, DE · Registration 3012010520

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
3012010520
FEI Number
3012010520
Entity Name
MEDIFA GMBH
City/State/Country
Finnentrop North Rhine-Westphalia, DE
Establishment Address
Industriestr. 5, Finnentrop North Rhine-Westphalia 57413, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
medifa GmbH (Owner Number: 10062007)
Owner / Operator Contact Address
Industriestr. 5, Finnentrop, DE-NW 57413, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

medifa 8000 800200 medifa 8000 800400

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IXR Table, Radiographic, Tilting Radiology Class 2 892.1980 2019-12-11

Official Correspondent

Hamdi Chalghaf

US Agent Details

Remo Rossi Business: Image Diagnostics Inc. Email: rrossi@imagediagnostics.com Phone: (978) 8290009

Related Public Records

Same Entity

medifa 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
K951176 Siemens Medical Solutions USA, Inc. KOORDINAT M 1995-04-20

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012010520. Last updated year: 2026. Please use registration number 3012010520 when referencing this establishment in official correspondence.
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