SAALMANN MEDICAL GMBH & CO. KG

FDA Device Registration & Listing · Bad Oeynhausen North Rhine-Westphalia, DE · Registration 3016463808

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
3016463808
FEI Number
3016463808
Entity Name
SAALMANN MEDICAL GMBH & CO. KG
City/State/Country
Bad Oeynhausen North Rhine-Westphalia, DE
Establishment Address
Suedbahnstrasse 34, Bad Oeynhausen North Rhine-Westphalia 32547, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Saalmann medical GmbH & Co. KG (Owner Number: 10062464)
Owner / Operator Contact Address
Suedbahnstrasse 34, Bad Oeynhausen, DE-NW 32547, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Saalio The Fischer

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 2020-01-30

Official Correspondent

Rolf Eilers

US Agent Details

Jennifer Jacobellis Business: Fischer Medical Supply Email: jen@arhinkel.com Phone: (818) 4700824

Related Public Records

Same Entity

Saalmann medical GmbH & Co. KG
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 3016463808. Last updated year: 2026. Please use registration number 3016463808 when referencing this establishment in official correspondence.
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