COAGULATION FACTOR XII - ANVISA Registration 80102511026
Access comprehensive regulatory information for COAGULATION FACTOR XII in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80102511026 and manufactured by DIAGNOSTICA STAGO S.A.S.. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS 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, 2 companies making the same product including ROCHE DIAGNOSTICS GMBH, TCOAG IRELAND LIMITED, and 2 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
80102511026
25351684417201139
04718143000194
Company Information
Dates and Status
Jan 31, 2012
VIGENTE
09/18/2025 19:00:01
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