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ANVISA registration 82195309012Active

PERIPHERAL ANGIOPLASTY BALLOON CATHETER

ANVISA Registration Number: 82195309012PURE LATAM BRAZIL COMERCIO DE PRODUTOS HOSPITALARES LTDAKOSSEL MEDTECH (SUZHOU) 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 com Balão PTA
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Risk class
Class II
Registration details
Registration Number
82195309012
Process Number
25351304726202445
CNPJ
27939884000109
Company information
Registration Holder
PURE LATAM BRAZIL COMERCIO DE PRODUTOS HOSPITALARES LTDA
Manufacturer
KOSSEL MEDTECH (SUZHOU) CO., LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Jun 17, 2024
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 82195309012 and manufactured by KOSSEL MEDTECH (SUZHOU) 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.