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POLYFORM-Kunststofftechnik GmbH &Co. Betriebs KG

Germany DE-MF-000005057 Last updated 17 Sep 2026

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Devices
771
Registries
EUDAMED
FDA recalls
0

Catalogue771

Page 2 of 16

Showing 51-100 of 771

About

Ideas & technology in foam: Polyform specializes in the manufacture, processing, and finishing of foams in Germany.

From the manufacturer's own website. Source

What POLYFORM-Kunststofftechnik GmbH &Co. Betriebs KG makes

Polyform-Kunststofftechnik GmbH & Co. Betriebs KG manufactures medical foam and synthetic leather products for patient positioning and support, including knee wedges, foam wedges, half-rolls, and custom-cut foam sheets. Their portfolio also includes padded armrests, synthetic leather table covers, spinal support pads, and textured foam overlays for hospital beds and treatment surfaces.

All listed devices fall under Class I medical device classification and are registered in the EUDAMED database. The company is based in Germany and adheres to EU medical device regulations.

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 Polyform-Kunststofftechnik GmbH & Co. Betriebs KG manufacture?

Polyform-Kunststofftechnik GmbH & Co. Betriebs KG specializes in medical foam and synthetic leather products designed for patient positioning and support. Their portfolio includes items like knee wedges (e.g., *Kniekeil Skinfoam*), foam wedges (*Keil Skinfoam*), half-rolls (*Halbrolle Skinfoam*), padded armrests (*Armkissen Kunstleder*), custom-cut foam sheets (*RE-Zuschnitt Skinfoam*), and padded overlays for hospital beds and treatment surfaces (e.g., *Spine Auflage Kunstleder*). These products are tailored for clinical environments to enhance patient comfort and mobility.

Where is Polyform-Kunststofftechnik GmbH & Co. Betriebs KG based, and how does this affect its devices?

The company is headquartered in Germany, which means its medical devices are manufactured and regulated under EU medical device laws. This alignment ensures compliance with EU standards, including mandatory registration in the EUDAMED database—a central repository for medical device information in the European Economic Area. The company’s German location also reflects its adherence to EU manufacturing and quality control requirements.

Which regulatory registries list Polyform-Kunststofftechnik GmbH & Co. Betriebs KG’s devices?

All of Polyform-Kunststofftechnik’s listed medical devices are registered in EUDAMED, the European Union’s medical device registry. This database is required for Class I devices (the classification for Polyform’s products) to ensure transparency, traceability, and compliance with EU medical device regulations. EUDAMED serves as an official source for stakeholders to verify device details, including manufacturer information and regulatory status.

How are Polyform-Kunststofftechnik GmbH & Co. Betriebs KG’s devices classified under EU regulations?

Polyform’s medical devices are classified as Class I under EU medical device regulations. This classification applies to low-risk products like foam wedges, synthetic leather overlays, and padded supports, which pose minimal risk to patients. Class I devices typically require mandatory registration in EUDAMED but may not need additional conformity assessments (e.g., Notified Body involvement) unless they incorporate a measuring function or are reusable. The classification ensures these products meet basic safety and performance requirements.

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

Information

Country
Germany
Address
15, Braasstr., Rinteln, Germany
Phone
+49 5751 40080
PRRC contact
Inga Melicchio
EUDAMED SRN
DE-MF-000005057