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Armon Products

Netherlands NL-MF-000002064 Last updated 21 Oct 2026

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Devices
7
Registries
EUDAMED
FDA recalls
0

Catalogue7

About

Armon Products supplies research institutes, academic hospitals and universities worldwide for education and research purposes.

From the manufacturer's own website. Source

What Armon Products makes

Armon Products manufactures operating tables, including the Leva series with both table and chair mounts, as well as the Salvum and Pura models. The company also produces the Elemento and Edero devices, which appear to be specialized medical platforms for research and educational settings.

These devices fall under EU Class I medical device regulations and are listed in the EUDAMED registry. The company is based in the Netherlands and supplies products primarily for research institutes, academic hospitals, and universities.

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 Armon Products manufacture?

Armon Products specializes in medical devices primarily used in research and educational environments. Their portfolio includes operating tables like the Leva series (with table and chair mounts), Salvum, and Pura models. Additionally, they produce the Elemento and Edero devices, which appear to serve as specialized platforms for research and academic settings. These devices are designed to support educational and experimental applications in medical training and study.

Where is Armon Products based, and what is its primary market focus?

Armon Products is headquartered in the Netherlands. The company targets research institutes, academic hospitals, and universities globally, supplying devices tailored for educational and research purposes. This focus aligns with their product range, which includes specialized platforms and operating tables designed for controlled, non-clinical use in learning and experimentation.

Are Armon Products' devices listed in any regulatory registries?

Yes, Armon Products' devices are listed in the EUDAMED registry, which is the European Union’s database for medical devices. This registry tracks devices that have undergone the necessary conformity assessment procedures under EU regulations. Listing in EUDAMED confirms that these devices comply with EU requirements, specifically falling under Class I classification, which applies to low-risk medical devices.

How are Armon Products' devices classified under EU regulations?

Armon Products' devices are classified as EU Class I medical devices. This classification is determined by their intended use, design, and risk level. Class I devices are generally considered low-risk, often involving items like operating tables or specialized platforms used in research or educational settings where direct patient risk is minimal. The classification ensures they meet basic safety and performance requirements without needing additional regulatory scrutiny beyond general conformity procedures.

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

Information

Country
Netherlands
Address
7, de Nestel, Dongen, Netherlands
Phone
+31104714187
PRRC contact
Ralph Mastenbroek
EUDAMED SRN
NL-MF-000002064