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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10350530144
Registration Details
ANVISA Registration Number: 10350530144
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

Cateter Guia Primum
Risk Class II

Registration Details

10350530144

25351000954201515

01197835000146

Company Information

Netherlands
PT: HOLANDA (PAĂŤSES BAIXOS)

Dates and Status

Jan 19, 2015

VIGENTE

09/18/2025 19:00:01