Pure Global AI
ANVISA registration 80174300024Active

Guide Wire

ANVISA Registration Number: 80174300024VALFLUX COMERCIO DE MATERIAIS HOSPITALARES LTDAVALFLUX GROUP, LLC.Risk Class II
Verified
Device names
Technical name
Guide Wire
View exact technical-name matches →
PT: Fio Guia
Commercial name
FIO-GUIA HIDROFÍLICO
View exact commercial-name matches →
Risk class
Class II
Registration details
Registration Number
80174300024
Process Number
25351183435201940
CNPJ
03872497000126
Company information
Registration Holder
VALFLUX COMERCIO DE MATERIAIS HOSPITALARES LTDA
Manufacturer
VALFLUX GROUP, LLC.
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Aug 26, 2019
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 80174300024 and manufactured by VALFLUX GROUP, LLC.. The registration is held by VALFLUX COMERCIO DE MATERIAIS HOSPITALARES LTDA with validity until currently active (VIGENTE).

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.