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ANVISA registration 80160719007Active

Guide Wire

ANVISA Registration Number: 80160719007PMF CARDIOLIFE IMPORTACAO E EXPORTACAO DE PRODUTOS MEDICOS LTDASHENZHEN MICROAPPROACH MEDICAL TECHNOLOGY CO., LTD.Risk Class II
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
Fio Guia Extra Stiff
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Risk class
Class II
Registration details
Registration Number
80160719007
Process Number
25351364539202411
CNPJ
04873446000181
Company information
Registration Holder
PMF CARDIOLIFE IMPORTACAO E EXPORTACAO DE PRODUTOS MEDICOS LTDA
Manufacturer
SHENZHEN MICROAPPROACH MEDICAL TECHNOLOGY CO., LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Jul 22, 2024
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 80160719007 and manufactured by SHENZHEN MICROAPPROACH MEDICAL TECHNOLOGY CO., LTD.. The registration is held by PMF CARDIOLIFE IMPORTACAO E EXPORTACAO 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.