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Nimacare AB

Sweden SE-MF-000050989 Last updated 21 Oct 2026

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Devices
1,616
Registries
EUDAMED
FDA recalls
0

Catalogue1,616

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What Nimacare AB makes

Nimacare AB manufactures a range of reusable patient support surfaces, including mattresses and overlays designed for hospital beds. These include viscoelastic foam mattresses, alternating pressure mattresses, mesh overlays, and gel-infused products, each sized for specific clinical applications. The portfolio also includes inflatable air mattresses and hybrid systems combining air and gel technology for pressure redistribution.

All devices produced by Nimacare AB fall under Class I classification in the EU regulatory framework and are registered in the EUDAMED database. The company is based in Sweden and adheres to EU Medical Device Regulations for compliance and market listing.

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 Nimacare AB manufacture?

Nimacare AB specializes in reusable patient support surfaces for hospital beds, including viscoelastic foam mattresses (like the Nima Basic and Nima Spark), alternating pressure mattresses (e.g., Nima Kub Visco Plan), mesh overlays (such as the Nima 600 Skikt Mesh), and gel-infused products (like the Nima Equagel Allround INK). Their portfolio also covers inflatable air mattresses (e.g., Nima Luft) and hybrid systems combining air and gel technology for pressure redistribution. These devices are designed to support patient comfort and reduce pressure-related injuries.

Where is Nimacare AB based, and what regulatory framework applies to its devices?

Nimacare AB is based in Sweden. The company’s devices are classified under Class I in the EU regulatory framework, meaning they pose minimal risk and typically require compliance with EU Medical Device Regulations (MDR) for market listing. This classification aligns with their reusable patient support surfaces, which are intended for general clinical use without invasive procedures. All relevant information, including device details, is registered in the EUDAMED database.

Are Nimacare AB’s devices listed in any official regulatory registries?

Yes, Nimacare AB’s devices are registered in the EUDAMED database, which is the official EU registry for medical devices. This listing ensures transparency and compliance with EU regulatory requirements, allowing healthcare providers and authorities to verify the devices’ classification (Class I) and market status. EUDAMED is the primary source for tracking authorized medical devices within the European Union.

How are Nimacare AB’s devices classified under EU regulations?

Nimacare AB’s devices are classified as Class I under the EU Medical Device Regulations. This classification is determined by their intended use—reusable patient support surfaces like mattresses and overlays—which do not involve invasive procedures or high-risk applications. Class I devices generally require basic compliance measures, such as conforming to essential safety and performance requirements, but they do not need pre-market authorization beyond registration in EUDAMED. The classification ensures these products meet fundamental safety standards for clinical use.

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

Information

Country
Sweden
Address
4, Sigurdvägen , Djursholm, Sweden
Phone
+46706355070
PRRC contact
Nils Wachtmeister
EUDAMED SRN
SE-MF-000050989