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ANVISA registration 80102513520Active

CORONARY ANGIOPLASTY BALLOON CATHETER

ANVISA Registration Number: 80102513520VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDAEUROCOR TECH GMBHRisk Class IV
Verified
Device names
Technical name
CORONARY ANGIOPLASTY BALLOON CATHETER
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PT: CATETER BALÃO PARA ANGIOPLASTIA CORONÁRIA
Commercial name
DIOR Cateter Balão PTCA Eluente de Paclitaxel
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Risk class
Class IV
Registration details
Registration Number
80102513520
Process Number
25351285515202404
CNPJ
04718143000194
Company information
Registration Holder
VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA
Manufacturer
EUROCOR TECH GMBH
Manufacturing Country
Germany
PT: ALEMANHA
Dates and status
Publication Date
Sep 15, 2025
Status
Active
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 80102513520 and manufactured by EUROCOR TECH GMBH. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Sep 15, 2035.

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.