Nimacare AB
Sweden SE-MF-000050989 Last updated 21 Oct 2026
- Devices
- 1,671
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Nima Förhöjningsdyna Coxit 1/4 Vändbar 45x45x5 cm Ref DFCK454550
Wheelchair Cushion Nima Ecoform Pluma 40x40 cm Ref ECOP4040
Wheelchair Cushion Nima Allround 621 40x45 cm Ref 6214045
Nima Equagel Standard 45x40 cm Ref NES4540
Nima Smart Gel Visco 45x42, 5 cm Ref SGV4542
Wheelchair Cushion Nima Allround 621 45x45 cm Ref 6214545
Nima Kub Visco Stöd 55x55 cm Ref KVS5555
Nima Kub Visco 42x50 cm Ref KV4250
Nima Kildyna Hård 40x40x8x1 cm Ref DKIHÅRD404081
Nima Kub Visco INK 33x30 cm Ref KVINK3330
Nima Smart Gel Visco 55x55 cm Ref SGV5555
Wheel Chair Cushion Nima Ecoform Pluma Skikt INK 35x35 cm Ref ECOPSINK3535
Nima Equagel Allround 50x45 cm Ref NEA5045
Wheelchair Cushion Nima Ecoform Pluma INK 35x33 cm Ref ECOPINK3533
Nima Förhöjningsdyna Coxit Halv 45x45x15 cm Ref DFCH454515
Nima Kub Visco 35x45 cm Ref KV3545
Nima Equagel Straight Comfort 42, 5x42, 5 cm Ref NESC4242
Nima Equagel Straight Comfort 42, 5x40 cm Ref NESC4240
Nima Smart Gel Visco 40x45 cm Ref SGV4045
Wheelchair Cushion Nima Ecoform Pluma 55x55 cm Ref ECOP5555
Nima Köksdyna Coxit Halv 43x40x7, 5 cm Ref DKCH434075
Showing 1,651-1,671 of 1,671
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.
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.
Information
- Country
- Sweden
- Address
- 4, Sigurdvägen , Djursholm, Sweden
- Website
- www.nimacare.se
- [email protected]
- Phone
- +46706355070
- PRRC contact
- Nils Wachtmeister
- EUDAMED SRN
- SE-MF-000050989