INTRAVASCULAR GUIDE CATHETER - ANVISA Registration 10350530068
Access comprehensive regulatory information for INTRAVASCULAR GUIDE CATHETER in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 10350530068 and manufactured by VASCULAR SOLUTIONS INC. The registration is held by LINE LIFE CARDIOVASCULAR COM DE PROD MED E HOSP LTDA with validity until Feb 28, 2026.
This page provides complete technical specifications for 2 related devices, 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
10350530068
25351084268201083
01197835000146
Company Information
Dates and Status
Feb 28, 2011
28/02/2026
09/18/2025 19:00:01
INTRAVASCULAR GUIDE CATHETER
Fio Guia InQwire
Merit Medical System, INC.
80740950012
Feb 15, 2016
GENERAL PURPOSE GUIDE WIRE, NON-VASCULAR
FIO GUIA PARA CPRE
WILSON-COOK MEDICAL INC/ COOK ENDOSCOPY
10212990108
May 21, 2004
Guide Wire
FIO-GUIA HIDROFĂŤLICO INT
SHANGHAI KINDLY MEDICAL INSTRUMENTS CO., LTD.
81582089006
Feb 03, 2022
Guide Wire
FIOS GUIA INDOVASIVE
BIORAD MEDISYS PRIVATE LIMITED
80459130001
Oct 05, 2009
Guide Wire
Fio Guia Periférico de Reentrada Enteer
EV3 INC.
10349000554
Feb 13, 2017
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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Not specified
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