Thorsis Technologies GmbH
Germany DE-MF-000017052 Last updated 21 Oct 2026
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- Devices
- 1
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
PlantaPress Ref 20020-0001
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.
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.
Information
- Country
- Germany
- Address
- 18, Oststraße, Magdeburg, Germany
- Website
- www.thorsis.com
- [email protected]
- Phone
- +49 391 544563 0
- PRRC contact
- Markus Fritzsche
- EUDAMED SRN
- DE-MF-000017052