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ANVISA registration 80102513682Valid until Jun 01, 2036

CORONARY ANGIOPLASTY BALLOON CATHETER

ANVISA Registration Number: 80102513682VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDABIOSENSORS EUROPE SARisk Class IV
Verified
Device names
Technical name
CORONARY ANGIOPLASTY BALLOON CATHETER
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PT: CATETER BALÃO PARA ANGIOPLASTIA CORONÁRIA
Commercial name
RISE™ SC
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Risk class
Class IV
Registration details
Registration Number
80102513682
Process Number
25351122786202522
CNPJ
04718143000194
Company information
Registration Holder
VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA
Manufacturer
BIOSENSORS EUROPE SA
Manufacturing Country
Switzerland
PT: SUÍÇA
Dates and status
Publication Date
Jun 01, 2026
Validity
01/06/2036
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for CORONARY ANGIOPLASTY BALLOON CATHETER in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80102513682 and manufactured by BIOSENSORS EUROPE SA. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Jun 01, 2036.

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.