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ANVISA registration 80202910103Active

Guide Wire

ANVISA Registration Number: 80202910103TECMEDIC COMÉRCIO DE PRODUTOS MÉDICOS LTDATOKAI MEDICAL PRODUCTS, INC.Risk Class II
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
Fio Guia M-Lead
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Risk class
Class II
Registration details
Registration Number
80202910103
Process Number
25351699892201951
CNPJ
05638301000169
Company information
Registration Holder
TECMEDIC COMÉRCIO DE PRODUTOS MÉDICOS LTDA
Manufacturer
TOKAI MEDICAL PRODUCTS, INC.
Manufacturing Country
Japan
PT: JAPÃO
Dates and status
Publication Date
Feb 17, 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 80202910103 and manufactured by TOKAI MEDICAL PRODUCTS, INC.. The registration is held by TECMEDIC COMÉRCIO DE PRODUTOS MÉDICOS 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.