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ANVISA registration 80446149015Active

PERIPHERAL ANGIOPLASTY BALLOON CATHETER

ANVISA Registration Number: 80446149015SMT IMPORTADORA E DISTRIBUIDORA DE PRODUTOS HOSPITALARES LTDA.ZHEJIANG BARTY MEDICAL TECHNOLOGY 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
Cateter Balão Ultra WANTY HP PTA - Duplo Lúmen
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Risk class
Class II
Registration details
Registration Number
80446149015
Process Number
25351881180202361
CNPJ
08862233000105
Company information
Registration Holder
SMT IMPORTADORA E DISTRIBUIDORA DE PRODUTOS HOSPITALARES LTDA.
Manufacturer
ZHEJIANG BARTY MEDICAL TECHNOLOGY CO., LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Jan 08, 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 80446149015 and manufactured by ZHEJIANG BARTY MEDICAL TECHNOLOGY CO., LTD.. The registration is held by SMT IMPORTADORA E DISTRIBUIDORA DE PRODUTOS HOSPITALARES 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.