COAGULATION FACTOR IV - ANVISA Registration 80003610568
Access comprehensive regulatory information for COAGULATION FACTOR IV in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80003610568 and manufactured by BIOKIT S/A. The registration is held by WERFEN MEDICAL LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 1 companies making the same product including DIAGNOSTICA STAGO S.A.S., and 1 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
80003610568
25351077639201942
02004662000165
Company Information
Dates and Status
Apr 08, 2019
VIGENTE
09/18/2025 19:00:01
Registration Details
80003610568
25351077639201942
02004662000165
Company Information
Dates and Status
Apr 08, 2019
VIGENTE
09/18/2025 19:00:01
COAGULATION FACTOR XIII
HemosIL Antígeno Fator XIII
IL INSTRUMENTATION LABORATORY
80003610320
Dec 24, 2012
VON WILLEBRAND COAGULATION FACTOR
HEMOSIL ANTIGENO FATOR DE VON WILLEBRAND
INSTRUMENTATION LABORATORY
80003610136
Feb 06, 2006
VON WILLEBRAND COAGULATION FACTOR
Hemosil Von Willebrand Fator Atividade
INSTRUMENTATION LABORATORY COMPANY
80003610361
Jul 08, 2013
VON WILLEBRAND COAGULATION FACTOR
Hemosil Von Willebrand Fator Ristocetina Cofator Atividade
INSTRUMENTATION LABORATORY COMPANY
80003610314
Dec 24, 2012
COAGULATION FACTOR IV
ASSERACHROM ® PF4
DIAGNOSTICA STAGO S.A.S.
80102510679
Aug 17, 2009