CG9063

Dénomination commerciale

non renseigné

06974323018759

B-06974323018759

Numéro de référence/catalogue

CG9063

GS1

IVDD — Général

Législation applicable

IVDD [Directive 98/79/CE relative aux dispositifs médicaux de diagnostic in vitro]

Statut

Sur le marché

Quantité

1

Description complémentaire du produit

The Rotavirus/Adenovirus/Norovirus Antigen Rapid Test Cassette is a lateral flow immunoassay intended use for qualitative detection of Rotavirus antigen, Adenovirus antigen and Norovirus antigen in stool samples. Rotavirus is one of the main pathogens that cause diarrhea. It mainly infects the epithelial cells of the small intestine, causing cell damage and diarrhea. Rotavirus is prevalent in summer, autumn and winter every year. The route of infection is the fecal-oral route. The course of the disease is generally 6-7 days, fever lasts 1-2 days, vomiting for 2 to 3 days, diarrhea for 5 days, and severe dehydration symptoms. Adenovirus is a particle with a diameter of 70 to 90 nm without an envelope. It is composed of 252 capsid particles arranged in a icosahedron shape. They can infect the respiratory tract, gastrointestinal tract, urethra and bladder, eyes, liver, etc. Adenovirus gastroenteritis is widely distributed all over the world. Norovirus is also known as Norwalk Viruses (NV) is the prototype representative strain of Norovirus (NV) in the Human Calicivirus (HuCV) family. It is a group of virus particles with similar morphology and slightly different antigenicity. Norovirus infectious diarrhea is prevalent all over the world, and infection can occur throughout the year. Norovirus infectious diarrhea is prevalent all over the world, and infection can occur throughout the year, with a high incidence in cold seasons.

URL des informations complémentaires

Aucune URL d'informations complémentaires renseignée par le fabricant.

Dimensions cliniques

Aucune dimension clinique enregistrée pour ce dispositif.

Nomenclature européenne des dispositifs médicaux — la classification produit UE attribuée à ce dispositif.

• W0105070399MULTIPLE VIRUSES - MULTIPLEX ASSAYS - OTHER