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ANVISA registration 82195309078Active

PERIPHERAL ANGIOPLASTY BALLOON CATHETER

ANVISA Registration Number: 82195309078PURE LATAM BRAZIL COMERCIO DE PRODUTOS HOSPITALARES LTDABEIJING DEMAX 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 de Dilatação por Balão ATP
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Risk class
Class II
Registration details
Registration Number
82195309078
Process Number
25351206003202562
CNPJ
27939884000109
Company information
Registration Holder
PURE LATAM BRAZIL COMERCIO DE PRODUTOS HOSPITALARES LTDA
Manufacturer
BEIJING DEMAX MEDICAL TECHNOLOGY CO.,LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Nov 17, 2025
Status
Active
Official value: VIGENTE
Last Updated
08/19/2026 19:00:01
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 82195309078 and manufactured by BEIJING DEMAX MEDICAL TECHNOLOGY CO.,LTD.. The registration is held by PURE LATAM BRAZIL COMERCIO 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.