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ANVISA registration 81884239013Active

Guide Wire

ANVISA Registration Number: 81884239013BHMEDICAL DISTRIBUICAO E IMPORTACAO DE PRODUTOS MEDICOS HOSPITALARES LTDASUNGJIN-HITECH CO., LTD.Risk Class II
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
Fio Guia Hidrofílico ANGUIS
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Risk class
Class II
Registration details
Registration Number
81884239013
Process Number
25351860946202373
CNPJ
31245991000104
Company information
Registration Holder
BHMEDICAL DISTRIBUICAO E IMPORTACAO DE PRODUTOS MEDICOS HOSPITALARES LTDA
Manufacturer
SUNGJIN-HITECH CO., LTD.
Manufacturing Country
South Korea
PT: CORÉIA DO SUL
Dates and status
Publication Date
Jan 15, 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 81884239013 and manufactured by SUNGJIN-HITECH CO., LTD.. The registration is held by BHMEDICAL DISTRIBUICAO E IMPORTACAO DE PRODUTOS MEDICOS 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.