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ANVISA registration 81284390002Active

Guide Wire

ANVISA Registration Number: 81284390002ROMED INDÚSTRIA E COMÉRCIO DE EQUIPAMENTOS MÉDICOS LTDAROMED EQUIPAMENTOS MEDICOS LTDA - EPPRisk Class I
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
FIO GUIA MANDRIL PARA ENTUBAÇÃO ROMED
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Risk class
Class I
Registration details
Registration Number
81284390002
Process Number
25351985555201629
CNPJ
13644713000130
Company information
Registration Holder
ROMED INDÚSTRIA E COMÉRCIO DE EQUIPAMENTOS MÉDICOS LTDA
Manufacturer
ROMED EQUIPAMENTOS MEDICOS LTDA - EPP
Manufacturing Country
Brazil
PT: BRASIL
Dates and status
Publication Date
May 30, 2016
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 I medical device is registered under ANVISA number 81284390002 and manufactured by ROMED EQUIPAMENTOS MEDICOS LTDA - EPP. The registration is held by ROMED INDÚSTRIA E COMÉRCIO DE EQUIPAMENTOS 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.