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ANVISA registration 80807430004Active

Guide Wire

ANVISA Registration Number: 80807430004MR MEDICAL COMÉRCIO DE EQUIPAMENTOS HOSPITALARES LTDAEPFLEX FEINWERKTECHNIK GMBHRisk Class II
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
Fio Guia Hidrofílico EPFlex
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Risk class
Class II
Registration details
Registration Number
80807430004
Process Number
25351263373201878
CNPJ
13233256000190
Company information
Registration Holder
MR MEDICAL COMÉRCIO DE EQUIPAMENTOS HOSPITALARES LTDA
Manufacturer
EPFLEX FEINWERKTECHNIK GMBH
Manufacturing Country
Germany
PT: ALEMANHA
Dates and status
Publication Date
May 21, 2018
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 80807430004 and manufactured by EPFLEX FEINWERKTECHNIK GMBH. The registration is held by MR MEDICAL COMÉRCIO DE EQUIPAMENTOS 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.