Guide Wire - ANVISA Registration 10210419005

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 10210419005 and manufactured by BROSMED MEDICAL CO., LTD. The registration is held by BIOASSIST COMERCIAL 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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10210419005
Registration Details
ANVISA Registration Number: 10210419005
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

fio guia hidrofilico
Risk Class II

Registration Details

10210419005

25351639782202155

40334484000120

Company Information

China
PT: CHINA, REPĂšBLICA POPULAR

Dates and Status

Jun 24, 2021

VIGENTE

09/18/2025 19:00:01