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ANVISA registration 82099939006Active

Guide Wire

ANVISA Registration Number: 82099939006SELLMED PRODUTOS MEDICOS E HOSPITALARES LTDASHUNMEI MEDICAL CO.,LTD.Risk Class II
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
Fio Guia Revestido Hidrofílico
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Risk class
Class II
Registration details
Registration Number
82099939006
Process Number
25351412803202430
CNPJ
37438274000177
Company information
Registration Holder
SELLMED PRODUTOS MEDICOS E HOSPITALARES LTDA
Manufacturer
SHUNMEI MEDICAL CO.,LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Oct 07, 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 82099939006 and manufactured by SHUNMEI MEDICAL CO.,LTD.. The registration is held by SELLMED PRODUTOS MEDICOS E HOSPITALARES 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.