Guide Wire - ANVISA Registration 81231550043
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 81231550043 and manufactured by Ningbo Multi-Way Medical Co. LTD.. The registration is held by Total Life comercio de produtos Medico-Hospitalar LTDA-EPP 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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Registration Details
81231550043
25351594784201811
21310535000139
Company Information
Dates and Status
Dec 17, 2018
VIGENTE
09/18/2025 19:00:01
Guide Wire
fio guia hidrofilico
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