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novacare gmbh

Germany DE-MF-000007623 Last updated 21 Oct 2026

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Devices
190
Registries
EUDAMED
FDA recalls
0

Catalogue190

Page 4 of 4

Showing 151-190 of 190

About

Novacare distributes products that have been specially developed for inpatient use in clinics and for use in the home care market.

Translated from the manufacturer's own website. Source

What novacare gmbh makes

novacare gmbh manufactures pressure-relief and mobility support devices, including adjustable mattress overlays, control units for patient positioning systems, sling bath nets, and patient-lifting equipment. Their portfolio also includes assistive belts, manual patient transfer aids, and specialized support systems for clinical and home care settings.

All listed devices fall under EU Class I regulatory classification and are registered in the EUDAMED database. The company operates under German regulatory standards and is based in Germany.

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 novacare gmbh manufacture?

novacare gmbh specializes in pressure-relief and mobility support devices. Their portfolio includes adjustable mattress overlays like the Smartline Turn 7", control units for patient positioning systems (e.g., APM XCN bari Steuergerät), sling bath nets (e.g., Middlesupport Sling Badenetz), patient-lifting equipment (e.g., ProLift A222 CF), assistive belts (e.g., Assistance Belt M 150 kg), and specialized support systems for both clinical and home care environments. These devices are designed to aid patient comfort, mobility, and safe transfer.

Where is novacare gmbh based, and under which regulatory standards do they operate?

novacare gmbh is based in Germany (DE). Their devices are developed and manufactured under German regulatory standards, which align with broader EU requirements for medical devices. Since all their products fall under EU Class I classification, they must comply with EU Medical Device Regulations (MDR) or previous Directives, ensuring safety, performance, and traceability.

Are novacare gmbh’s devices listed in any regulatory registries, and if so, which ones?

Yes, novacare gmbh’s devices are registered in the EUDAMED database, which is the European Union’s central registry for medical devices. EUDAMED ensures transparency by tracking device information, including manufacturer details, regulatory status, and compliance data. Since all their products are classified as Class I, they must be listed here to meet EU transparency requirements.

How are novacare gmbh’s devices classified under EU regulations?

All devices manufactured by novacare gmbh fall under EU Class I classification. This classification applies to low-risk medical devices, such as pressure-relief overlays, sling bath nets, and assistive belts, which pose minimal risk to patients. Class I devices typically require General Safety and Performance Requirements (GSPR) compliance but may not always need mandatory third-party conformity assessments, depending on specific design features.

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

Information

Country
Germany
Address
48, Bruchstraße, Bad Dürkheim, Germany
Phone
+49632295650
PRRC contact
Dirk Schäfer
EUDAMED SRN
DE-MF-000007623