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ANVISA registration 81504790153Active

Guide Wire

ANVISA Registration Number: 81504790153PASSROD IMPORTAÇÃO E EXPORTAÇÃO DE PRODUTOS PARA SAÚDE LTDA - MEOPTIMED - MEDIZINISCHE INSTRUMENTE GMBHRisk Class II
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
GUIDE WIRE NITINOL - FIO GUIA
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Risk class
Class II
Registration details
Registration Number
81504790153
Process Number
25351200448202024
CNPJ
26185222000110
Company information
Registration Holder
PASSROD IMPORTAÇÃO E EXPORTAÇÃO DE PRODUTOS PARA SAÚDE LTDA - ME
Manufacturer
OPTIMED - MEDIZINISCHE INSTRUMENTE GMBH
Manufacturing Country
Germany
PT: ALEMANHA
Dates and status
Publication Date
Apr 20, 2020
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 81504790153 and manufactured by OPTIMED - MEDIZINISCHE INSTRUMENTE GMBH. The registration is held by PASSROD IMPORTAÇÃO E EXPORTAÇÃO DE PRODUTOS PARA SAÚDE LTDA - ME 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.