COAGULATION FACTOR V - ANVISA Registration 80502070032

Access comprehensive regulatory information for COAGULATION FACTOR V in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80502070032 and manufactured by MOBIUS LIFE SCIENCE INDÚSTRIA E COMERCIO DE PRODUTOS PARA LABORATÓRIOS LTDA. The registration is held by MOBIUS LIFE SCIENCE INDUSTRIA E COMERCIO DE PRODUTOS PARA LABORATORIOS 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 INSTRUMENTATION LABORATORY CO., ROCHE DIAGNOSTICS GMBH, 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
80502070032
Registration Details
ANVISA Registration Number: 80502070032
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

XGEN MASTER Fator V - Kit Master para Detecção Alélica de Fator V de Leiden
Risk Class II

Registration Details

80502070032

25351711421201590

04645160000149

Dates and Status

Apr 25, 2016

VIGENTE

09/18/2025 19:00:01