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ROTAVIRUS - ANVISA Registration 81325990299

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 81325990299 and manufactured by HANGZHOU ALLTEST BIOTECH CO. LTD. The registration is held by QR CONSULTING, IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS LTDA 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, GUANGZHOU WONDFO 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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81325990299
Registration Details
ANVISA Registration Number: 81325990299
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Device Details

Família Teste Rápido para Detecção do Combo Rotavírus e Adenovírus em Cassete (Fezes)
Risk Class II

Registration Details

81325990299

25351512199202360

19933144000129

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Sep 04, 2023

VIGENTE

09/18/2025 19:00:01