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ANVISA registration 81231550085Valid until Sep 15, 2035

Guide Wire

ANVISA Registration Number: 81231550085Total Life comercio de produtos Medico-Hospitalar LTDA-EPPSHANGHAI INT MEDICAL INSTRUMENTS CO.,LTD.Risk Class IV
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
Fio guia para Angioplastia
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Risk class
Class IV
Registration details
Registration Number
81231550085
Process Number
25351377601202434
CNPJ
21310535000139
Company information
Registration Holder
Total Life comercio de produtos Medico-Hospitalar LTDA-EPP
Manufacturer
SHANGHAI INT MEDICAL INSTRUMENTS CO.,LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Sep 15, 2025
Validity
15/09/2035
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 IV medical device is registered under ANVISA number 81231550085 and manufactured by SHANGHAI INT MEDICAL INSTRUMENTS CO.,LTD.. The registration is held by Total Life comercio de produtos Medico-Hospitalar LTDA-EPP with validity until Sep 15, 2035.

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.