HIDREX GMBH

FDA Device Registration & Listing · Heiligenhaus North Rhine-Westphalia, DE · Registration 3008642982

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
3008642982
FEI Number
3008642982
Entity Name
HIDREX GMBH
City/State/Country
Heiligenhaus North Rhine-Westphalia, DE
Establishment Address
Otto-Hahn-Str. 12, Heiligenhaus North Rhine-Westphalia 42579, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Hidrex GmbH (Owner Number: 10049191)
Owner / Operator Contact Address
Otto-Hahn-Str. 12, Heiligenhaus, DE-NW 42579, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K133033
PMA Number
N/A

All Registered Proprietary Names

HIDREX DVP1000 Aquex DAAV1000 HIDREX DP450 Phothera Aquex (HIPRO10)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EGJ Device, Iontophoresis, Other Uses Physical Medicine Class 2 890.5525 2015-04-27

Official Correspondent

Andreas Kaemper

US Agent Details

Stefanie D. Bankston Email: vigilance@beoberlin.eu Phone: (713) 4834617

Related Public Records

Same Entity

Hidrex 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
K842483 Santa Barbara Medco, Inc. SANTA BARBARA MEDCO-LANTOPHORETIC APPLIC 1984-08-31

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008642982. Last updated year: 2026. Please use registration number 3008642982 when referencing this establishment in official correspondence.
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