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ANVISA registration 80202919023Active

PERIPHERAL ANGIOPLASTY BALLOON CATHETER

ANVISA Registration Number: 80202919023TECMEDIC COMÉRCIO DE PRODUTOS MÉDICOS LTDACNOVATE MEDICAL B.VRisk Class II
Verified
Device names
Technical name
PERIPHERAL ANGIOPLASTY BALLOON CATHETER
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PT: CATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA
Commercial name
Cateter Balão Não Complacente
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Risk class
Class II
Registration details
Registration Number
80202919023
Process Number
25351046473202561
CNPJ
05638301000169
Company information
Registration Holder
TECMEDIC COMÉRCIO DE PRODUTOS MÉDICOS LTDA
Manufacturer
CNOVATE MEDICAL B.V
Manufacturing Country
Netherlands
PT: HOLANDA (PAÍSES BAIXOS)
Dates and status
Publication Date
Apr 14, 2025
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 80202919023 and manufactured by CNOVATE MEDICAL B.V. The registration is held by TECMEDIC COMÉRCIO DE PRODUTOS 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.