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ANVISA registration 81403789002Active

Guide Wire

ANVISA Registration Number: 81403789002ARQUIMED DISTRIBUIDORA E REPRESENTACAO DE PRODUTOS MEDICOS LTDAACE MEDICAL DEVICES PVT. LTD. (EAST AVENUE)Risk Class II
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
Fio Guia Hidrofílico ACE
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Risk class
Class II
Registration details
Registration Number
81403789002
Process Number
25351178479202334
CNPJ
23241814000113
Company information
Registration Holder
ARQUIMED DISTRIBUIDORA E REPRESENTACAO DE PRODUTOS MEDICOS LTDA
Manufacturer
ACE MEDICAL DEVICES PVT. LTD. (EAST AVENUE)
Manufacturing Country
India
PT: ÍNDIA
Dates and status
Publication Date
Apr 03, 2023
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 81403789002 and manufactured by ACE MEDICAL DEVICES PVT. LTD. (EAST AVENUE). The registration is held by ARQUIMED DISTRIBUIDORA E REPRESENTACAO DE PRODUTOS MEDICOS 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.