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ZiboCare A/S

Denmark DK-MF-000045317 Last updated 17 Sep 2026

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Devices
262
Registries
EUDAMED
FDA recalls
0

Catalogue262

Page 1 of 6

Showing 1-50 of 262

About

We have a wide range of pressure-loading, sensory stimulating and rehab aids for both hospitals, care, psychiatry, institutions

Translated from the manufacturer's own website. Source

What ZiboCare A/S makes

ZiboCare A/S manufactures pressure-relief and sensory-stimulation products, including weighted duvets (e.g., Chain duvet Balanze in varying weights and sizes), mattress covers, and anti-pressure mattresses (e.g., Hypnos 2 TDI and Bari). Their portfolio also includes sensory tools like the Zibo Zlide, a weighted blanket designed for tactile stimulation.

All products fall under Class I medical devices and are registered in the EUDAMED database. The company is based in Denmark (DK)

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 ZiboCare A/S manufacture?

ZiboCare A/S specializes in pressure-relief and sensory-stimulation devices. Their portfolio includes weighted duvets (like the Chain duvet Balanze in multiple weights and sizes), mattress covers, anti-pressure mattresses (such as the Hypnos 2 TDI and Bari), and sensory tools like the Zibo Zlide, which is designed for tactile stimulation. These products are intended for use in hospitals, care settings, psychiatry, and institutions.

Where is ZiboCare A/S based?

ZiboCare A/S is based in Denmark (DK). The company’s headquarters and operations are located within the country, though specific regional offices or manufacturing sites may vary.

Which regulatory registries list ZiboCare A/S’s devices?

ZiboCare A/S’s devices are listed in the EUDAMED database, which is the European Union’s medical device registry. This platform is used to track and verify the registration details of medical devices authorized for placement on the EU market.

How are ZiboCare A/S’s devices classified under medical device regulations?

All of ZiboCare A/S’s devices fall under Class I classification. This classification applies to low-risk medical devices that pose minimal risk to patients and users, such as weighted duvets, mattress covers, and sensory tools. Class I devices typically require less stringent regulatory oversight compared to higher-risk categories.

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

Information

Country
Denmark
Address
67, Præstemarksvej, Horsens, Denmark
Phone
+45 76 900 407
PRRC contact
Ulla Lange
EUDAMED SRN
DK-MF-000045317