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ANVISA registration 80963580018Active

Guide Wire

ANVISA Registration Number: 80963580018MEDICAL NORDESTE IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS LTDAEPFLEX FEINWERKTECHNIK GMBHRisk Class II
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
Fio Guia Hidrofílico Lifeline
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Risk class
Class II
Registration details
Registration Number
80963580018
Process Number
25351375826201581
CNPJ
17017519000185
Company information
Registration Holder
MEDICAL NORDESTE IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS LTDA
Manufacturer
EPFLEX FEINWERKTECHNIK GMBH
Manufacturing Country
Germany
PT: ALEMANHA
Dates and status
Publication Date
Sep 14, 2015
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 80963580018 and manufactured by EPFLEX FEINWERKTECHNIK GMBH. The registration is held by MEDICAL NORDESTE IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS 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.