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Guide Wire - ANVISA Registration 10330719029

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 10330719029 and manufactured by SHENZHEN MICROAPPROACH MEDICAL TECHNOLOGY CO., LTD.. The registration is held by HANDLE COMERCIO DE EQUIPAMENTOS MEDICOS 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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10330719029
Registration Details
ANVISA Registration Number: 10330719029
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Device Details

Fio Guia Hidrofílico Zebrado PTFE - UroEssence
Risk Class II

Registration Details

10330719029

25351048110202560

54756242000139

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Apr 22, 2025

VIGENTE

09/18/2025 19:00:01