Guide Wire - ANVISA Registration 80174309027

Access comprehensive regulatory information for 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 80174309027 and manufactured by YILSON MEDICAL TECHNOLOGY CO., LTD.. The registration is held by VALFLUX COMERCIO DE MATERIAIS HOSPITALARES 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 E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME, SP MEDICAL A/S, 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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80174309027
Registration Details
ANVISA Registration Number: 80174309027
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

FIO-GUIA teflonado
Risk Class II

Registration Details

80174309027

25351662145202182

03872497000126

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jul 01, 2021

VIGENTE

09/18/2025 19:00:01