Guide Wire - ANVISA Registration 10312210042

Access comprehensive regulatory information for Guide Wire in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10312210042 and manufactured by Martech Medical Product. The registration is held by MEDCORP SAUDE TECNOLOGIA LTDA with validity until currently active (VIGENTE).

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 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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10312210042
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Registration Details
ANVISA Registration Number: 10312210042
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

FIO GUIA
Risk Class I

Registration Details

10312210042

25351410557201342

67630541000174

Company Information

Mexico
PT: MÉXICO

Dates and Status

Oct 21, 2013

VIGENTE

09/18/2025 19:00:01

FIO GUIA
Risk Class I

Registration Details

10312210042

25351410557201342

67630541000174

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Oct 21, 2013

VIGENTE

09/18/2025 19:00:01