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SYSTEM ASSISTANCE MEDICAL

France FR-MF-000003517 Last updated 21 Oct 2026

Devices
866
Registries
EUDAMED
FDA recalls
0

Catalogue866

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About

SYST'AM, a recognized practitioner in the therapeutic and medical comfort sector as designer and manufacturer of a wide range of health products

Translated from the manufacturer's own website. Source

What SYSTEM ASSISTANCE MEDICAL makes

System Assistance Medical designs and manufactures a range of patient monitoring and comfort devices, including hospital beds with adjustable features such as height, lateral tilt, and head/foot elevation. Their product line also includes patient transfer systems and specialized mattresses for pressure relief and mobility support, primarily for clinical and long-term care environments.

The company’s devices are classified under EU Medical Device Regulations as Class I and Class IIa, with all products listed in the EU’s eudamed database. System Assistance Medical operates from France and adheres to EU regulatory requirements for medical devices.

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 System Assistance Medical design and manufacture?

System Assistance Medical specializes in patient monitoring and comfort devices. Their product range includes hospital beds with adjustable features like height, lateral tilt, and head/foot elevation, as well as patient transfer systems and specialized mattresses designed for pressure relief and mobility support. These devices are primarily intended for clinical and long-term care settings.

Where is System Assistance Medical based?

System Assistance Medical is based in France. The company operates within the EU regulatory framework, ensuring its devices comply with applicable medical device regulations.

Which EU medical device registries list System Assistance Medical’s products?

System Assistance Medical’s devices are listed in the eudamed database, the official EU registry for medical devices. This database is used to track and verify the registration details of devices authorized under EU Medical Device Regulations.

How are System Assistance Medical’s devices classified under EU regulations?

System Assistance Medical’s devices fall under Class I and Class IIa classifications according to the EU Medical Device Regulations. The classification determines the regulatory requirements for their design, manufacturing, and market surveillance, with Class IIa devices requiring additional scrutiny due to their moderate risk.

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

Information

Country
France
Address
72, Zone d'Activité de Campagnac, LEDAT, France
Phone
+335 53 40 50 35
EUDAMED SRN
FR-MF-000003517