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DISCHER Technik GmbH

Germany·DE-MF-000004972

Last updated September 18, 2026

About

High-tech disinfection for safe hygiene in medicinetechnik ? Alten- & Nursing home? Hospital? Top rated? 02104 2336 0

Translated from the manufacturer's own website. Source

What DISCHER Technik GmbH makes

DISCHER Technik GmbH manufactures automated disinfection systems for medical equipment, including models such as the DISCHER Boy, DISCHER Compact, and DISCHER Piccolo series. These devices are designed for high-efficiency cleaning and disinfection of medical instruments, surgical tools, and other reusable medical devices in clinical and care settings. The portfolio also includes larger systems like the DISCHER Master and DISCHER Boy Plus, tailored for high-volume or specialized disinfection needs.

The company’s disinfection systems fall under EU medical device Class IIa classification and are registered in the EU’s eudamed database. The manufacturer is based in Germany and adheres to relevant EU regulatory requirements for medical device compliance.

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 DISCHER Technik GmbH manufacture?

DISCHER Technik GmbH specializes in automated disinfection systems for medical equipment. These devices are designed to clean and disinfect reusable medical instruments, surgical tools, and other clinical items used in hospitals, nursing homes, and care facilities. Examples include the DISCHER Boy, DISCHER Compact, DISCHER Piccolo, and larger systems like the DISCHER Master and DISCHER Boy Plus, all tailored for high-efficiency hygiene in healthcare settings.

Where is DISCHER Technik GmbH based, and what regulatory requirements do its devices follow?

DISCHER Technik GmbH is based in Germany. Its devices are developed and marketed in compliance with EU medical device regulations, including classification under the EU’s medical device framework. The company ensures its products meet the necessary safety, performance, and hygiene standards for use in clinical environments.

Which regulatory registries list DISCHER Technik GmbH’s devices?

DISCHER Technik GmbH’s devices are registered in the eudamed database, which is the official EU registry for medical devices. This listing ensures transparency and traceability of its automated disinfection systems under EU regulatory oversight.

How are DISCHER Technik GmbH’s disinfection systems classified under EU regulations?

DISCHER Technik GmbH’s disinfection systems fall under EU Class IIa classification. This classification is assigned based on the risk associated with the device’s intended use, where Class IIa represents a moderate risk level requiring additional scrutiny to ensure safety and performance in disinfecting medical equipment.

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

Information

Country
Germany
Address
4-6, Fuhr, Haan, Germany
LinkedIn
—
Facebook
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Phone
+49 2104 2336-0
PRRC Contact
Anja Discher
EUDAMED SRN
DE-MF-000004972
FDA FEI Number
—
DUNS Number
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Catalogue (8)

DeviceModel / ReferenceRegistriesClassStatus
DISCHER Boy 20212 / 20213
EUDAMED
Class IIaActive
DISCHER Compact 20220
EUDAMED
Class IIaActive
DISCHER Master S 20208 / 20209 / 20210 / 20211
EUDAMED
Class IIaActive
DISCHER Piccolo S 20224 / 20225 / 20226 / 20227
EUDAMED
Class IIaActive
DISCHER Boy S 20214 / 20215 / 20216 / 20217
EUDAMED
Class IIaActive
DISCHER Piccolo 20222 / 20223
EUDAMED
Class IIaActive
DISCHER Master 20204 / 20205 / 20206 / 20207
EUDAMED
Class IIaActive
DISCHER Boy Plus 20218 / 20219
EUDAMED
Class IIaActive

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