ArcDia International Oy Ltd
Finland FI-MF-000007553 Last updated 21 Oct 2026
- Devices
- 53
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
mariPOC® Sample tube Ref A-1
mariPOC® Analyser Ref AD7-020
mariPOC® Pharyn test plate Ref 1124M
mariPOC® SARS-CoV-2 test reagent Ref 1R13
mariPOC® Extraction solution B Ref B03B
mariPOC® Extraction solution A Ref B03A
mariPOC® SARS-CoV-2 test plate Ref 1204S
mariPOC® Gastro CDI combi test plate Ref 2027M
mariPOC® Quick combi+ test plate Ref 1214M
mariPOC® Respi test plate Ref 1154M
mariPOC® Respi+ test plate Ref 1184M
mariPOC® Bottletop dispenser stand Ref A-29
mariPOC® RTI control samples Ref 1104MC
mariPOC® Test plate storage rack Ref A-43
mariPOC® RTI combi+ test plate Ref 1194M
mariPOC® Quick Flu+ test plate Ref 1224M
mariPOC® Gastro test plate Ref 2017M
mariPOC® Gastro sample buffer Ref B06
mariPOC® Inactivation solution Ref B07
mariPOC® Gastro control samples Ref 2017MC
mariPOC® System solution Ref B05
mariPOC® Quick Flu+ control samples Ref 1224MC
mariPOC® Pharyn control samples Ref 1124MC
mariPOC® RTI sample buffer Ref B02
mariPOC® RTI combi test plate Ref 1164M
mariPOC® Sample tube cap Ref A-2
mariPOC® Respi test plate Ref 1114M
mariPOC® CDI test plate Ref 2037M
mariPOC® Software Ref AD1-S
mariPOC® SARS-2 control samples Ref 1204SC
mariPOC® Quick combi test plate Ref 1174M
mariPOC® Rotavirus test reagent Ref 2R07
mariPOC® Filtration unit rack Ref A-44
mariPOC® Wash solution Ref B04
Showing 1-50 of 53
About
mariPOC® test system enables fast and accurate diagnosis in acute infections. Multiple pathogens are tested from a single clinical sample simultaneously.
What ArcDia International Oy Ltd makes
ArcDia International Oy Ltd manufactures in vitro diagnostic (IVD) test systems for rapid pathogen detection, including sample tubes, analysers, test plates, and reagents. These products are designed for diagnosing acute infections, such as respiratory viruses (e.g., SARS-CoV-2, parainfluenza, respiratory syncytial virus) and bacterial infections (e.g., Group A streptococcus, *Clostridioides difficile*). The system allows simultaneous testing of multiple pathogens from a single clinical sample.
The company’s IVD devices fall under Class A and IVD General device classifications, with all products listed in the EU’s eudamed registry. The portfolio is regulated under EU IVD Regulation (IVDR) standards, ensuring compliance with diagnostic accuracy and safety requirements. The manufacturer is based in Finland.
Information
- Country
- Finland
- Address
- 32, Lemminkäisenkatu , Turku, Finland
- Website
- www.arcdia.com/
- [email protected]
- Phone
- +358406787414
- PRRC contact
- Mikko Tasanen
- EUDAMED SRN
- FI-MF-000007553