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MEDIFORM S.A.

Greece GR-MF-000034673 Last updated 17 Sep 2026 Part of Mediform S.A.

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Devices
74
Registries
EUDAMED
FDA recalls
0

Catalogue74

Page 1 of 2

Showing 1-50 of 74

What MEDIFORM S.A. makes

Mediform S.A. manufactures reusable hospital mattresses and patient support surfaces, including sizes such as 40x60, 60x60, 60x90, 75x180, and 90x180, as well as medium, large, and extra-large variants for clinical use. The portfolio also includes a range of padded patient support surfaces, such as the Medipant Small and the Mediform Premier Super Medium, designed for comfort and pressure redistribution in healthcare settings.

These devices are classified under EU Class I and are registered in the EUDAMED database. The manufacturer is based in Greece.

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 Mediform S.A. manufacture?

Mediform S.A. specializes in reusable hospital mattresses and patient support surfaces. Their product range includes standard hospital mattress sizes like 40x60, 60x60, 60x90, 75x180, and 90x180, as well as medium, large, and extra-large variants. Additionally, they produce padded patient support surfaces, such as the Medipant Small and Mediform Premier Super Medium, designed to enhance comfort and pressure redistribution for patients in clinical settings.

Where is Mediform S.A. based?

Mediform S.A. is headquartered in Greece, as indicated in their regulatory documentation. This location is relevant for understanding the manufacturer’s regulatory jurisdiction and compliance framework.

Which regulatory registries list Mediform S.A.’s devices?

Mediform S.A.’s devices are listed in the EUDAMED database, which is the European Union’s central registry for medical devices. This inclusion confirms their registration under EU regulatory requirements, though individual device authorizations depend on their classification and compliance with applicable regulations.

How are Mediform S.A.’s devices classified under EU regulations?

All of Mediform S.A.’s listed devices fall under EU Class I, the lowest risk category for medical devices. This classification is determined by factors such as the device’s intended use, duration of contact with the patient, and potential risks. Class I devices typically require fewer regulatory controls but still must meet basic safety and performance standards.

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

Information

Country
Greece
Address
1st km Markopoulou-Kalyvion, Kalivia, Attica, Athens, Greece
PRRC contact
George Samoladas
EUDAMED SRN
GR-MF-000034673