Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

Merivaara Corporation

Finland·FI-MF-000001175

Last updated September 18, 2026

About

Merivaara Group is a forerunner in intuitive healthcare technology and industrial design, with surgery room solutions being a key focus and growth area.

From the manufacturer's own website. Source

What Merivaara Corporation makes

Merivaara Corporation manufactures medical accessories and equipment for clinical and surgical environments, including leg rest pairs, wrist straps, anesthesia screens, drainage bowls, and side rails. Their portfolio also includes flow measurement devices like the Q-Flow series, as well as control units for surgical procedures and patient monitoring systems.

All products fall under EU Class I medical devices and are registered in the EUDAMED database. The company is based in Finland and adheres to EU regulatory requirements for Class I devices.

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 Merivaara Corporation manufacture?

Merivaara Corporation produces a range of medical accessories and equipment primarily designed for clinical and surgical settings. Their portfolio includes items like leg rest pairs, wrist straps, anesthesia screens, drainage bowls, side rails, and flow measurement devices such as the Q-Flow series. Additionally, they offer control units for surgical procedures and patient monitoring systems, all tailored to support healthcare environments.

Where is Merivaara Corporation based?

Merivaara Corporation is headquartered in Finland. The company’s location aligns with EU regulatory frameworks, ensuring compliance with European medical device standards for the products it manufactures.

Which regulatory registries list Merivaara Corporation’s devices?

Merivaara Corporation’s medical devices are listed in the EUDAMED database, which is the European Union’s medical device registry. This registry tracks devices authorised under EU regulations, including those classified under Class I.

How are Merivaara Corporation’s devices classified under EU regulations?

All of Merivaara Corporation’s devices fall under EU Class I classification. This classification is typically assigned to low-risk medical devices, such as accessories and simple monitoring tools, where the risk to patient safety is minimal. Class I devices must still comply with EU regulatory requirements, including design controls, manufacturing standards, and traceability in registries like EUDAMED.

Why are Merivaara Corporation’s devices listed in EUDAMED if they’re Class I?

Even though Class I devices are considered lower risk, EU regulations mandate that all medical devices—regardless of class—must be registered in EUDAMED to ensure transparency, traceability, and compliance with EU directives. This includes details like device identification, manufacturer information, and classification, which helps healthcare providers, regulators, and patients access accurate data about authorised products.

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

Information

Country
Finland
Address
2-4, Tarmontie, Hollola, Finland
Facebook
—
Phone
+3585408439755
PRRC Contact
—
EUDAMED SRN
FI-MF-000001175
FDA FEI Number
—
DUNS Number
—

Catalogue (54)

Page 2 of 2
DeviceModel / ReferenceRegistriesClassStatus
Arthroscopic stress post MV-12530 100012530
EUDAMED
Class IActive
Side Support 120 100000120
EUDAMEDFDA UDI
Class IActive
Q-Flow TRIO 520230
EUDAMED
Class IActive
Q-Flow 1 Cm Long Range 52010311
EUDAMED
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Merivaara Oy US