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NOROVIRUS - ANVISA Registration 80277090050

Access comprehensive regulatory information for NOROVIRUS in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80277090050 and manufactured by ACRO – BIOTECH, INC. The registration is held by GRIMEXTUR- IMPORTAÇÃO E EXPORTAÇÃO DO BRASIL LTDA ME with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including R-BIOPHARM AG, HYSEN BIOTECH.LNC, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.

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80277090050
Registration Details
ANVISA Registration Number: 80277090050
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Device Details

Teste Rápido para Norovírus (Fezes)
Risk Class II

Registration Details

80277090050

25351809321202156

07236937000100

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jan 14, 2021

VIGENTE

09/18/2025 19:00:01