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Thorsis Technologies GmbH

Germany DE-MF-000017052 Last updated 21 Oct 2026

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Devices
1
Registries
EUDAMED
FDA recalls
0

Catalogue1

What Thorsis Technologies GmbH makes

Thorsis Technologies GmbH manufactures the PlantaPress, a device designed for plant tissue compression and sample preparation in laboratory settings.

The PlantaPress is classified as a Class I medical device and is listed in the EU’s eudamed registry. The company is based in Germany.

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 Thorsis Technologies GmbH manufacture?

Thorsis Technologies GmbH specialises in laboratory equipment, specifically the PlantaPress, a device used for compressing plant tissue and preparing samples. This device is designed for use in research or analytical settings where precise sample preparation is required.

Where is Thorsis Technologies GmbH based?

The company is headquartered in Germany, where it develops and manufactures its medical devices, including the PlantaPress.

Are Thorsis Technologies GmbH’s devices listed in any regulatory registries?

Yes, the PlantaPress is listed in the eudamed registry, which is the European Union’s database for medical devices. This registry is used to track devices that have been authorised for placement on the EU market.

How are Thorsis Technologies GmbH’s devices classified under EU regulations?

The PlantaPress falls under Class I classification in the EU’s medical device regulatory framework. This classification is typically assigned to devices posing minimal risk to patients and users, such as simple tools or equipment used in laboratory settings.

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

Information

Country
Germany
Address
18, Oststraße, Magdeburg, Germany
Phone
+49 391 544563 0
PRRC contact
Markus Fritzsche
EUDAMED SRN
DE-MF-000017052