ROTAVIRUS - ANVISA Registration 82890930003
Access comprehensive regulatory information for ROTAVIRUS in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82890930003 and manufactured by R-BIOPHARM AG. The registration is held by R-BIOPHARM BRASIL COMERCIO DE PRODUTOS PARA ANALISE DE ALIMENTOS LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including GUANGZHOU WONDFO BIOTECH CO. LTD, HANGZHOU ALLTEST BIOTECH CO., LTD, 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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Registration Details
82890930003
25351445925202411
67272757000296
Company Information
Dates and Status
Jan 27, 2025
VIGENTE
09/18/2025 19:00:01
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Família Teste Rápido para Detecção do Combo Rotavírus e Adenovírus em Cassete (Fezes)
HANGZHOU ALLTEST BIOTECH CO. LTD
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Kit de teste de antígeno do grupo A de Rotavírus (RV) (método do ouro coloidal)
ZHUHAI KEYU BIOLOGICAL ENGINEERING CO., LTD.
81778810012
Jun 05, 2023