Nimacare AB
Sweden SE-MF-000050989 Last updated 21 Oct 2026
- Devices
- 1,671
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Nima 621 Tät 45x45 cm Ref 621TÄT4545
Nima Allround Skikt 50x50 cm Ref 621SKIKT5050
Nima 600 MESH INK 53x50 cm Ref 600MESHINK5350
Nima 600 Tät Mesh 37x35 cm Ref 600TM3735
Nima Kub Visco Plan INK 47x40 cm Ref KVPINK4740
Nima Kub Visco Plan INK 45x45 cm Ref KVPINK4545
Nima Allround MESH INK 30x33 cm Ref 621MESHINK3033
Nima Plan Kupad INK 40x45 cm Ref NPKINK4045
Nima Kub Visco Stöd INK 40x40 cm Ref KVSINK4040
Nima Kub Visco Plan 45x55 cm Ref KVP4555
Nima 600 Visco INK 60x60 cm Ref 600VISCOINK6060
Nima Ecoform Pluma Rundad 37x35 cm Ref ECOPR3735
Nima Basic INK 65x55 cm Ref NBINK6555
Nima Allround MESH INK 55x50 cm Ref 621MESHINK5550
Nima Kub Visco Plan INK 40x50 cm Ref KVPINK4050
Nima Basic 40x42, 5 cm Ref NB4042
Nima 600 Tät 55x50 cm Ref 600T5550
Nima Allround Skikt Mesh INK 55x55 cm Ref 621SKIKTMESHINK5555
Nima 600 TÄT INK 47x45 cm Ref 600TINK4745
Nima 600 Skikt INK 37x35 cm Ref 600SKIKTINK3735
Nima 600 Skikt Mesh INK 47x47 cm Ref 600SKIKTMESHINK4747
Nima 600 PU 33x30 cm Ref 600PU3330
Nima 600 Skikt Tät 40x42 cm Ref 600ST4042
Nima 600 Visco INK 65x65 cm Ref 600VISCOINK6565
Nima Luft Hög 33x33 cm Ref NIMALH3333
Nima Equagel Allround INK 40x40 cm Ref NEAINK4040
Nima 600 Positionering INK 42x42 cm Ref 600PINK4242
Nima 600 TÄT INK 53x55 cm Ref 600TINK5355
Nima Luft Hög 42x40 cm Ref NIMALH4240
Nima Spark 53x55 cm Ref 600SPARK5355
Nima Allround Skikt Mesh 30x30 cm Ref 621SKIKTMESH3030
Nima 600 TÄT INK 37x35 cm Ref 600TINK3735
Nima Allround Skikt Mesh 42x40 cm Ref 621SKIKTMESH4240
Nima Luft Hög INK 30x33 cm Ref NIMALHINK3033
Nima Allround MESH INK 53x55 cm Ref 621MESHINK5355
Nima Ecoform Pluma Rundad INK 37x33 cm Ref ECOPRINK3733
Nima 600 MESH INK 40x42, 5 cm Ref 600MESHINK4042
Nima Smart Gel Visco INK 40x42, 5 cm Ref SGVINK4042
Nima 600 Positionering INK 60x55 cm Ref 600PINK6055
Nima Equagel Allround INK 50x40 cm Ref NEAINK5040
Nima Spark 50x45 cm Ref 600SPARK5045
Nima 600 Tät 45x40 cm Ref 600T4540
Nima 600 TÄT INK 37x40 cm Ref 600TINK3740
Nima Allround Skikt 40x42 cm Ref 621SKIKT4042
Nima Ecoform Pluma Rundad INK 50x40 cm Ref ECOPRINK5040
Nima 600 Visco INK 35x35 cm Ref 600VISCOINK3535
Nima Allround Skikt INK 30x30 cm Ref 621SKIKTINK3030
Nima 600 Tät 40x42 cm Ref 600T4042
Nima Allround MESH INK 47x43 cm Ref 621MESHINK4743
Nima Kub Visco Plan INK 30x30 cm Ref KVPINK3030
Showing 201-250 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