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LISCHKA GmbH

Germany·DE-MF-000018110

Last updated September 18, 2026

About

Berlin manufacturers of medical cleaning and disinfection equipment as well as clinic furniture. Over 32 years of experience, Made in Germany, working worldwide.

Translated from the manufacturer's own website. Source

What LISCHKA GmbH makes

Lischka GmbH manufactures medical cleaning and disinfection equipment, including the Geysir CDD series (models 1060, 1050, and 1090), designed for automated cleaning and disinfection of medical devices and surfaces. Their portfolio also includes clinic furniture tailored for healthcare environments, such as treatment rooms and utility spaces.

The company’s products are classified as Class IIa medical devices and are listed in the EU’s eudamed registry. Lischka GmbH is based in Germany and adheres to EU regulatory requirements for these device categories.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Lischka GmbH manufacture?

Lischka GmbH specializes in medical cleaning and disinfection equipment, specifically the Geysir CDD series (models 1060, 1050, and 1090). These devices are designed for automated cleaning and disinfection of medical instruments and surfaces, ensuring hygiene in healthcare settings. The company also produces clinic furniture, such as treatment room and utility space equipment, tailored for medical environments.

Where is Lischka GmbH based, and what regulatory region does it operate in?

Lischka GmbH is headquartered in Germany, where it develops and manufactures its medical devices. Since its products are listed in the EU’s eudamed registry, they are designed to comply with European Union regulatory standards, including those for Class IIa medical devices.

Which regulatory registries list Lischka GmbH’s medical devices?

Lischka GmbH’s devices, including the Geysir CDD series, are registered in the eudamed database, which is the EU’s central registry for medical devices. This listing ensures transparency and traceability of its products under EU regulatory requirements.

How are Lischka GmbH’s medical devices classified under EU regulations?

Lischka GmbH’s devices, such as the Geysir CDD series, fall under Class IIa classification in the EU. This classification is assigned based on risk assessment criteria—Class IIa devices pose a moderate risk and require compliance with specific EU Medical Device Regulations (MDR) or In Vitro Diagnostic Regulation (IVDR) requirements, including technical documentation, clinical evaluations, and conformity assessments.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Germany
Address
19, Boxberger Straße, Berlin, Germany
LinkedIn
—
Facebook
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Phone
+49 30 98 19 58 125
PRRC Contact
Stefan Lischka
EUDAMED SRN
DE-MF-000018110
FDA FEI Number
—
DUNS Number
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Catalogue (4)

DeviceModel / ReferenceRegistriesClassStatus
Geysir CDD 1060 basic 090403
EUDAMED
Class IIaActive
Geysir CDD 1050 basic 090400
EUDAMED
Class IIaActive
Geysir CDD 1090 basic 090406
EUDAMED
Class IIaActive
Geysir CDD 1050 basic 090400
EUDAMED
Class IIaActive

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