Eu Ivdd Eu Ivd General On The Market 🇫🇮 Finland

mariPOC® Rotavirus test reagent

ArcDia International Oy Ltd · 🇫🇮 Finland
Devices (same UDI-DI)
1
Certificates
0
Countries
0
Notified Bodies
0

Basic Information

Primary DI
D-2R07EY
Basic UDI-DI Code
B-2R07EY
Reference
2R07
Device Types
None provided
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

The test reagent devices consist of polystyrene microparticles as a solid phase carrier coated with affinity binders, such as monoclonal or polyclonal antibodies. specific for the analyte (antigen), and fluorescent affinity binder, such as monoclonal or polyclonal antibody, conjugates as a tracer. The immunoassay active components are dried with protective sugars and buffer components inside individual reaction chambers on test configuration packages. The mariPOC® Rotavirus test reagent is intended to be used for the detection of rotavirus antigens when there is a suspicion of acute gastroenteritis. The function of the device is for screening and/or aid to diagnosis in order to provide specific information on the physiological state by providing limited information on the microbiological content of the specimen. Intended specimen type is native (unprocessed) human feces. The use of the device is automated and the device is stored in dry format inside mariPOC® test plate reaction wells. The results are reported qualitatively as positive (+) or negative (−) on the graphical user interface of the mariPOC® Software.

CND Nomenclature Codes

Code Description
W0105040606 ROTAVIRUS

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