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Guide Wire - ANVISA Registration 83058639013

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 83058639013 and manufactured by SUZHOU RUIZHUOYUAN MEDICAL SCI & TECH CO. LTD. The registration is held by BRAZIL REGULATORY 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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83058639013
Registration Details
ANVISA Registration Number: 83058639013
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Device Details

Fio guia Hidrofílico GDM
Risk Class II

Registration Details

83058639013

25351131025202561

51593659000130

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Aug 04, 2025

VIGENTE

09/18/2025 19:00:01