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Guide Wire - ANVISA Registration 80770619001

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 80770619001 and manufactured by EUROS S.A.S.. The registration is held by ANGEL CARE SOLUCOES E INOVACOES PARA MEDICINA 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 Mร‰DICO-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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80770619001
Registration Details
ANVISA Registration Number: 80770619001
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Device Details

FIOS GUIA EUROS
Risk Class II

Registration Details

80770619001

25351183407202228

08800570000178

Company Information

EUROS S.A.S.
France
PT: FRANร‡A

Dates and Status

Apr 20, 2022

VIGENTE

09/18/2025 19:00:01