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Tukimet Oy

Finland FI-MF-000006700 Last updated 21 Oct 2026

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Devices
132
Registries
EUDAMED
FDA recalls
0

Catalogue132

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About

Tukimet Oy on Raumalla toimiva monipuolisia Tyke -apuvälineitä valmistava tuotantolaitos.

From the manufacturer's own website. Source

What Tukimet Oy makes

Tukimet Oy manufactures mobility and hygiene aids for individuals with limited mobility, including adjustable shower chairs, viscoelastic wheelchair cushions in various sizes, hip protection cushions, support rails, motorized bed lifts with rotating and low-floor designs, freestanding shower chairs with hygiene openings, transport models of shower chairs, walking frames, and wooden floor-lift risers for hospital beds.

The company’s products are classified as Class I medical devices and are listed in the EU’s eudamed registry. Tukimet Oy is based in Rauma, Finland.

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 Tukimet Oy manufacture?

Tukimet Oy specializes in mobility and hygiene aids designed for individuals with limited mobility. Their product range includes adjustable shower chairs, viscoelastic wheelchair cushions in multiple sizes, hip protection cushions, support rails, motorized bed lifts with rotating and low-floor designs, freestanding shower chairs with hygiene openings, transport models of shower chairs, walking frames, and wooden floor-lift risers for hospital beds. These devices are intended to assist with independence, safety, and comfort in daily activities.

Where is Tukimet Oy based?

Tukimet Oy is based in Rauma, Finland. The company operates as a manufacturing facility focused on producing mobility and hygiene aids tailored for users with limited mobility.

Which regulatory registries list Tukimet Oy’s devices?

Tukimet Oy’s devices are listed in the EU’s eudamed registry, which is the central database for medical device information under EU regulations. This registry ensures transparency and traceability of devices authorized for use within the European Economic Area.

How are Tukimet Oy’s devices classified under medical device regulations?

All of Tukimet Oy’s devices fall under Class I classification. This classification applies to low-risk medical devices, such as mobility aids and hygiene supports, which typically do not require invasive procedures or sustained use. Class I devices are subject to basic safety and performance requirements but may still need conformity assessment procedures depending on their specific design and intended use.

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

Information

Country
Finland
Address
33, Kaivopuistontie, Rauma, Finland
Phone
+35826774222
PRRC contact
Jani Hiljanen
EUDAMED SRN
FI-MF-000006700