CARDIOVASCULAR GUIDE WIRE - ANVISA Registration 10341350821

Access comprehensive regulatory information for CARDIOVASCULAR GUIDE WIRE in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 10341350821 and manufactured by LAKE REGION MEDICAL. The registration is held by BOSTON SCIENTIFIC DO BRASIL LTDA with validity until Jun 01, 2035.

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 ABBOTT MEDICAL, COOK INCORPORATED, 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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10341350821
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Registration Details
ANVISA Registration Number: 10341350821
Janaina dos Santos de Miranda

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Related Devices (2)

FIO GUIA SAFARI PRE-SHAPED TAVR/TAVI
Risk Class IV

Registration Details

10341350821

25351449941201472

01513946000114

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jun 01, 2015

01/06/2035

09/18/2025 19:00:01

FIO GUIA SAFARI PRE-SHAPED TAVR/TAVI
Risk Class IV

Registration Details

10341350821

25351449941201472

01513946000114

Company Information

Dates and Status

Jun 01, 2015

01/06/2035

09/18/2025 19:00:01