ANVISA registration 80019169023Active

Guide Wire

Name: Guide Wire — ANVISA registration 80019169023
Creator: SOLUMED MATERIAIS MÉDICOS LTDA
Keywords: Guide Wire, Fio Guia, Fio guia hidrofílico, 80019169023, Risk Class II, ANVISA registration

ANVISA Registration Number: 80019169023SOLUMED MATERIAIS MÉDICOS LTDASOLUMED MATERIAIS MÉDICOS LTDARisk Class II

Verified

Device names

Technical name: Guide Wire
Commercial name: Fio guia hidrofílico
Risk class: Class II

Registration details

Registration Number: 80019169023
Process Number: 25351115449202589
CNPJ: 01000823000180

Company information

Registration Holder: SOLUMED MATERIAIS MÉDICOS LTDA
Manufacturer: SOLUMED MATERIAIS MÉDICOS LTDA
Manufacturing Country: Brazil

Dates and status

Publication Date: Jul 21, 2025
Validity: VIGENTE
Last Updated: 08/18/2026 19:00:00

About this record

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 80019169023 and manufactured by SOLUMED MATERIAIS MÉDICOS LTDA. The registration is held by SOLUMED MATERIAIS MÉDICOS LTDA with validity until currently active (VIGENTE).

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