ROTAVIRUS - ANVISA Registration 80464810625

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 80464810625 and manufactured by EPITOPE DIAGNOSTICS. The registration is held by ARGOSLAB DISTRIBUIDORA DE PRODUTOS PARA LABORATÓRIOS 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 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Similar Products
5 Competitors
80464810625
Registration Details
ANVISA Registration Number: 80464810625
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

🇧🇷 Brazil Regulatory Expert

Need help with your Brazil registration?

Contact Pure Global Brazil Team
Free consultation

Device Details

EDI Fecal Rotavirus Antigen ELISA Kit
Risk Class II

Registration Details

80464810625

25351585067201890

09377976000152

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Feb 04, 2019

VIGENTE

09/18/2025 19:00:01