INTRAVASCULAR GUIDE CATHETER - ANVISA Registration 10350530144
Access comprehensive regulatory information for INTRAVASCULAR GUIDE CATHETER in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10350530144 and manufactured by PENDRACARE INTERNATIONAL B.V.. The registration is held by LINE LIFE CARDIOVASCULAR COM DE PROD MED E HOSP 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 TERUMO CORPORATION, BOSTON SCIENTIFIC CORPORATION - MARLBOROUGH, 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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Registration Details
10350530144
25351000954201515
01197835000146
Company Information
Dates and Status
Jan 19, 2015
VIGENTE
09/18/2025 19:00:01
INTRAVASCULAR GUIDE CATHETER
Fio Guia InQwire
Merit Medical System, INC.
80740950012
Feb 15, 2016
CARDIOVASCULAR GUIDE WIRE
GUIA AQWIRE
EV3. INC
10349000458
Jun 22, 2015
CARDIOVASCULAR GUIDE WIRE
FIO GUIA PARA PTCA
BALTON LTD
80120820010
Feb 20, 2006
CARDIOVASCULAR GUIDE WIRE
FIO GUIA PARA PTCA
Not specified
80120820010
Feb 20, 2006
CARDIOVASCULAR GUIDE WIRE
GUIDE RIGHT FIO GUIA
ABBOTT MEDICAL
10332340140
Apr 29, 2005
TERUMO CORPORATION• Japan
BOSTON SCIENTIFIC CORPORATION - MARLBOROUGH• United States of America
ASAHI INTECC CO.,LTD• Japan
CORDIS CORPORATION• United States of America
PENUMBRA, INC.• United States of America
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