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Claus Andersen, Rustfrit Stål A/S

Denmark DK-MF-000048409 Last updated 17 Sep 2026

Devices
2
Registries
EUDAMED
FDA recalls
0

Catalogue2

About

Specialister i rustfrit stål til storkøkkener og maskinindustrien. Kontakt Claus Andersen Rustfri Stål for skræddersyede løsninger.

From the manufacturer's own website, in their original language. Source

What Claus Andersen, Rustfrit Stål A/S makes

Claus Andersen, Rustfrit Stål A/S manufactures stainless steel defibrillator cabinets designed for medical use, providing durable enclosures for automated external defibrillators.

These devices fall under EU Class I medical device classification and are registered in the EU’s eudamed database. The company is based in Denmark.

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 Claus Andersen, Rustfrit Stål A/S manufacture?

Claus Andersen, Rustfrit Stål A/S specializes in manufacturing stainless steel defibrillator cabinets. These are specifically designed as durable enclosures for automated external defibrillators, ensuring protection and stability for medical use.

Where is Claus Andersen, Rustfrit Stål A/S based?

The company is based in Denmark, operating as Claus Andersen, Rustfrit Stål A/S. Its location in Denmark aligns with EU regulatory frameworks, which govern the classification and registration of its medical devices.

Which regulatory registries list the defibrillator cabinets manufactured by Claus Andersen, Rustfrit Stål A/S?

The defibrillator cabinets produced by Claus Andersen, Rustfrit Stål A/S are listed in the EU’s eudamed database. This registry is the official EU portal for medical device information, ensuring transparency and traceability for authorized devices.

How are the defibrillator cabinets manufactured by Claus Andersen, Rustfrit Stål A/S classified under EU regulations?

The defibrillator cabinets fall under EU Class I medical device classification. This classification is determined by factors such as the risk associated with the device’s intended use and its design. Class I devices are generally considered low-risk, but they still require compliance with EU medical device regulations.

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

Information

Country
Denmark
Address
8, Fabriksvej, Odense S, Denmark
Phone
+4563950500(from company website)
PRRC contact
Heidi Storm Rasmussen
EUDAMED SRN
DK-MF-000048409