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Journalia AB

Active in EUDAMED

Swedenfrom SRN EUDAMED SRN SE-MF-000042926

Devices
1
Registrations
EUDAMED

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor

What Journalia AB makes

Journalia AB manufactures the AKnet, a medical device designed for monitoring and managing acute kidney injury (AKI) in critical care settings. The system integrates continuous renal replacement therapy (CRRT) monitoring and data analytics to support clinical decision-making and patient outcomes in intensive care units.

The AKnet is classified as a Class IIa medical device under EU regulations and is listed in the EUDAMED database. The company is based in Sweden.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • AKnet

    Class IIa
    Active CE MDR EUDAMED IIa

Company details

EUDAMED SRN
SE-MF-000042926
EU VAT number
SE556482514801
EUDAMED status
Active
EUDAMED registered name
Journalia AB
Registered address
77, Gunnerud, 68696, Östra Ämtervik, Sweden
Phone
+46 554 22231
PRRC contact
Helen Sandelin(public in EUDAMED)

Frequently asked questions

How many devices does Journalia AB have in the registry?

The registry currently lists 1 device for Journalia AB. Devices recorded under merged duplicate company entries are counted once.

Which registries list Journalia AB's devices?

Among its 1 most recently registered device, Journalia AB has devices listed in EUDAMED (1 device).

What risk classes do Journalia AB's devices fall under?

Among its 1 most recently registered device, the classes recorded for Journalia AB's devices are Class IIa. Each device page shows its own class and authorisation.

What are the newest devices from Journalia AB in the registry?

The most recently registered devices listed for Journalia AB include AKnet.

Generated automatically from registry data and not verified by a human reviewer.