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
Catalogue
Keil Skinfoam blau 200x280x140/2 mm Ref 151602
Keil Skinfoam blau 36x24x7/1cm Ref 110940
Kniekissen Skinfoam blau 320x202x40 mm Ref 139658
Tischauflage Kunstleder ocean 225x75x2 cm Ref 151742
Kissen Skinfoam blau 102x49x2 cm Ref 124386-01
Dreieck Skinfoam blau 54x24x12 cm Ref 120719
Dreieck Skinfoam blau 44x71/15x16 cm Ref 150808
Keilkissen Kunstleder ocean 178x279x76/2 mm Ref 149698
Lagerungsbank Skinfoam gelb 13x11x8 cm Ref 111034
Rechteck Skinfoam violett 36x24x5 cm Ref 103846
RE-Zuschnitt Skinfoam blau 500x450x15 mm Ref 146105
Lagerungskissen Skinfoam blau 290x190x55 mm Ref 100070-01
Kniekissen Skinfoam blau 365x160x67 mm Ref 139659
Fersenstütze Skinfoam blau 360x170/140/35 mm Ref 146706
Lagerungsrolle Skinfoam blau Ø 22x60 cm Ref 142365
Armlagerung Skinfoam blau 150x445x90/45mm Ref 158488
Ring geprägt blau Ø 20/5x5 cm Ref 108576
Dreieck Skinfoam gelb 60x30x15 cm Ref 120541
Showing 751-771 of 771
About
Ideas & technology in foam: Polyform specializes in the manufacture, processing, and finishing of foams in Germany.
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.
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.
Information
- Country
- Germany
- Address
- 15, Braasstr., Rinteln, Germany
- Website
- www.polyform.de
- [email protected]
- Phone
- +49 5751 40080
- PRRC contact
- Inga Melicchio
- EUDAMED SRN
- DE-MF-000005057