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ANVISA registration 83032659011Active

Guide Wire

ANVISA Registration Number: 83032659011SAINT GERMAIN COMERCIAL LTDAMANISH MEDI INNOVATIONRisk Class II
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
FIO GUIA HIDROFÍLICO
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Risk class
Class II
Registration details
Registration Number
83032659011
Process Number
25351126693202577
CNPJ
12115576000183
Company information
Registration Holder
SAINT GERMAIN COMERCIAL LTDA
Manufacturer
MANISH MEDI INNOVATION
Manufacturing Country
India
PT: ÍNDIA
Dates and status
Publication Date
Aug 04, 2025
Status
Active
Official value: VIGENTE
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 83032659011 and manufactured by MANISH MEDI INNOVATION. The registration is held by SAINT GERMAIN COMERCIAL 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.