Pure Global AI
ANVISA registration 81487669009Active

Guide Wire

ANVISA Registration Number: 81487669009GF MEDIKA IMPORTAÇÃO E EXPORTAÇÃO LTDASHANGHAI INT MEDICAL INSTRUMENTS CO.,LTD.Risk Class II
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
ProT™ Fio Guia
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Risk class
Class II
Registration details
Registration Number
81487669009
Process Number
25351231797202501
CNPJ
20503395000152
Company information
Registration Holder
GF MEDIKA IMPORTAÇÃO E EXPORTAÇÃO LTDA
Manufacturer
SHANGHAI INT MEDICAL INSTRUMENTS CO.,LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Jan 05, 2026
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 81487669009 and manufactured by SHANGHAI INT MEDICAL INSTRUMENTS CO.,LTD.. The registration is held by GF MEDIKA IMPORTAÇÃO E EXPORTAÇÃO 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.