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ANVISA registration 80788629004Active

PERIPHERAL ANGIOPLASTY BALLOON CATHETER

ANVISA Registration Number: 80788629004NIPRO MEDICAL CORPORATION PRODUTOS MÉDICOS LTDAGOODMAN CO., LTD.Risk Class II
Verified
Device names
Technical name
PERIPHERAL ANGIOPLASTY BALLOON CATHETER
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PT: CATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA
Commercial name
Finestream S Plus PTA Baloon Dilatation Catheter
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Risk class
Class II
Registration details
Registration Number
80788629004
Process Number
25351436977202498
CNPJ
13333090000184
Company information
Registration Holder
NIPRO MEDICAL CORPORATION PRODUTOS MÉDICOS LTDA
Manufacturer
GOODMAN CO., LTD.
Manufacturing Country
Japan
PT: JAPÃO
Dates and status
Publication Date
Dec 09, 2024
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 80788629004 and manufactured by GOODMAN CO., LTD.. The registration is held by NIPRO MEDICAL CORPORATION 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.