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ANVISA registration 81325990100Active

Guide Wire

ANVISA Registration Number: 81325990100QR CONSULTING, IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS LTDABIOMETRIX LTDRisk Class II
Verified
Device names
Technical name
Guide Wire
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PT: Fio Guia
Commercial name
Fio Guia Amplatz Biometrix
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Risk class
Class II
Registration details
Registration Number
81325990100
Process Number
25351202499201957
CNPJ
19933144000129
Company information
Registration Holder
QR CONSULTING, IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS LTDA
Manufacturer
BIOMETRIX LTD
Manufacturing Country
Israel
PT: ISRAEL
Dates and status
Publication Date
Sep 16, 2019
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 81325990100 and manufactured by BIOMETRIX LTD. The registration is held by QR CONSULTING, IMPORTACAO E DISTRIBUICAO 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.