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Guide Wire - ANVISA Registration 10309090032

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 10309090032 and manufactured by INSITU TECHNOLOGIES, INC. The registration is held by CLINICAL THINKS COMÉRCIO DE PROD. E EQUIP. CIRÚRGICOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 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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10309090032
Registration Details
ANVISA Registration Number: 10309090032
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Device Details

Fio Guia Lobella
Risk Class II

Registration Details

10309090032

25351306794201809

85472199000103

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Aug 20, 2018

VIGENTE

09/18/2025 19:00:01