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ANVISA registration 81487669001Active

PERIPHERAL ANGIOPLASTY BALLOON CATHETER

ANVISA Registration Number: 81487669001GF MEDIKA IMPORTAÇÃO E EXPORTAÇÃO LTDAQMEDICS AGRisk Class II
Verified
Device names
Technical name
PERIPHERAL ANGIOPLASTY BALLOON CATHETER
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PT: CATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA
Commercial name
Balão BTK QMedics
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Risk class
Class II
Registration details
Registration Number
81487669001
Process Number
25351278097202067
CNPJ
20503395000152
Company information
Registration Holder
GF MEDIKA IMPORTAÇÃO E EXPORTAÇÃO LTDA
Manufacturer
QMEDICS AG
Manufacturing Country
Switzerland
PT: SUÍÇA
Dates and status
Publication Date
Oct 29, 2020
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for PERIPHERAL ANGIOPLASTY BALLOON CATHETER in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81487669001 and manufactured by QMEDICS AG. The registration is held by GF MEDIKA IMPORTAÇÃO E EXPORTAÇÃO 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.