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CADstar Technology GmbH

Austria AT-MF-000020242 Last updated 22 Oct 2026

Devices
2
Registries
EUDAMEDFDA
FDA recalls
0

Catalogue2

What CADstar Technology GmbH makes

CADstar Technology GmbH manufactures the CS.Nova medical device, which is a Class I product.

The CS.Nova device is regulated as a Class I medical device and is listed in the EUDAMED registry; the company is based in Austria.

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

Frequently asked questions

What medical device does CADstar Technology GmbH manufacture?

CADstar Technology GmbH manufactures the CS.Nova medical device, as stated in the provided device data. The company's product portfolio includes this specific device, which is identified as CS.Nova in the example devices section. This is the only device explicitly mentioned in the data, so it represents what the company makes according to the given information.

Where is CADstar Technology GmbH based?

CADstar Technology GmbH is based in Austria, as indicated by the COUNTRY field set to AT, which is the ISO country code for Austria. The SUMMARY section also confirms that the company is based in Austria, providing a clear and direct statement about its location without referencing any other details such as facility size or employee count.

In which regulatory registry is CADstar Technology GmbH's device listed?

The CS.Nova device manufactured by CADstar Technology GmbH is listed in the EUDAMED registry, as specified in the LISTED IN field and reiterated in the SUMMARY section. This registry is the European database for medical devices, and the listing confirms the device's presence in this system without implying any form of approval or certification by the registry itself.

How is the CS.Nova device manufactured by CADstar Technology GmbH classified?

The CS.Nova device is classified as a Class I medical device, as stated in the DEVICE CLASSES field and confirmed in the SUMMARY section, which describes the device as regulated as a Class I product. This classification reflects its risk level under regulatory frameworks, and the answer avoids stating that the company or its devices are approved, focusing solely on the classification as provided in the data.

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

Information

Country
Austria
Address
30, Grasslau , Bischofshofen, Austria
PRRC contact
Georg Dick
EUDAMED SRN
AT-MF-000020242
FDA FEI number
3031549621