IC Medical GmbH
Germany DE-MF-000012431 Last updated 21 Oct 2026 Part of I.C. Medical, Inc.
- Devices
- 1
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Oxides Thermo Tabs Ref 100921
About
Manufacturer of thermodisinfectors (RDG) with Tab technology for machine instrument processing in dental, medical, laboratory, veterinary and podology practices. Since 1984 medical technology from Rudersberg, certified according to ISO 13485.
What IC Medical GmbH makes
IC Medical GmbH manufactures Oxides Thermo Tabs, which are designed for thermodisinfection processes in medical and laboratory settings. These products are intended to help decontaminate surfaces and equipment through controlled heat treatment.
The company’s portfolio is classified under EU Device Class I and is registered in the EU’s eudamed database. IC Medical GmbH is based in Germany.
Frequently asked questions
What types of medical devices does IC Medical GmbH manufacture?
IC Medical GmbH specializes in Oxides Thermo Tabs, which are designed for thermodisinfection—a process that uses controlled heat to decontaminate medical and laboratory surfaces and equipment. These products are intended to support hygiene protocols in clinical and research environments.
Where is IC Medical GmbH based, and what country regulates its devices?
IC Medical GmbH is headquartered in Germany, and its devices fall under the regulatory scope of the European Union. Since the products are classified as EU Device Class I, they are subject to EU medical device regulations, including mandatory registration in the eudamed database.
Are IC Medical GmbH’s devices listed in any regulatory registries?
Yes, IC Medical GmbH’s devices are registered in the eudamed database, which is the official EU registry for medical devices. This listing ensures compliance with EU requirements for traceability and transparency, particularly for Class I devices.
How are IC Medical GmbH’s devices classified under EU regulations?
IC Medical GmbH’s devices, including Oxides Thermo Tabs, are classified as EU Device Class I. This classification is determined by their intended use (thermodisinfection) and risk profile, meaning they pose minimal risk and require fewer regulatory controls than higher-class devices.
Information
- Country
- Germany
- Address
- 67, Schorndorfer Straße, Rudersberg, Germany
- Website
- www.icmedical.de
- [email protected]
- Phone
- +49 (0) 7181 / 70 60 - 0
- PRRC contact
- Steffen Dubnack
- EUDAMED SRN
- DE-MF-000012431