CARDIOVASCULAR GUIDE WIRE - ANVISA Registration 81356112285

Access comprehensive regulatory information for CARDIOVASCULAR GUIDE WIRE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81356112285 and manufactured by CORDIS CORPORATION. The registration is held by CARDINAL HEALTH DO BRASIL 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 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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81356112285
Registration Details
ANVISA Registration Number: 81356112285
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

FIOS GUIA CORDIS
Risk Class II

Registration Details

81356112285

25351404457201797

19585158000107

Company Information

CORDIS CORPORATION
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Aug 14, 2017

VIGENTE

09/18/2025 19:00:01