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Kallies Feinchemie AG

Active in EUDAMED

Germanyfrom SRN EUDAMED SRN DE-MF-000025918

Devices
1
Registrations
EUDAMED

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor

What Kallies Feinchemie AG makes

Kallies Feinchemie AG produces Lugol’s solution, a pharmaceutical-grade iodine preparation used for medical applications such as wound care and diagnostic testing.

The company’s products are classified as Class A medical devices and are registered in the EU’s eudamed database. The manufacturer is based in Germany.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Lugols-Lösung Ref 6321

    Active Regimes: CE IVDR Registry: EUDAMED Class:A

Company details

EUDAMED SRN
DE-MF-000025918
EU VAT number
DE 140635598
EUDAMED status
Active
EUDAMED registered name
Kallies Feinchemie AG
EUDAMED abbreviated name
Kallies Feinchemie AG
Registered address
9, Höhenweg, 01855, Sebnitz, Germany
Phone
0359715060
PRRC contact
Claudia Seidel(public in EUDAMED)

Frequently asked questions

How many devices does Kallies Feinchemie AG have in the registry?

The registry currently lists 1 device for Kallies Feinchemie AG. Devices recorded under merged duplicate company entries are counted once.

Which registries list Kallies Feinchemie AG's devices?

Among its 1 most recently registered device, Kallies Feinchemie AG has devices listed in EUDAMED (1 device).

What risk classes do Kallies Feinchemie AG's devices fall under?

Among its 1 most recently registered device, the classes recorded for Kallies Feinchemie AG's devices are IVDR Class A. Each device page shows its own class and authorisation.

What are the newest devices from Kallies Feinchemie AG in the registry?

The most recently registered devices listed for Kallies Feinchemie AG include Lugols-Lösung.

Generated automatically from registry data and not verified by a human reviewer.