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ANVISA registration 80898209025Active

PERIPHERAL ANGIOPLASTY BALLOON CATHETER

ANVISA Registration Number: 80898209025LAIBO MEDICAL PRODUTOS MEDICOS E HOSPITALARES LTDAHIWIN MEDTECH (SHENZHEN) 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
HP PTA Balloon - HiwinMed
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Risk class
Class II
Registration details
Registration Number
80898209025
Process Number
25351100002202696
CNPJ
14477127000100
Company information
Registration Holder
LAIBO MEDICAL PRODUTOS MEDICOS E HOSPITALARES LTDA
Manufacturer
HIWIN MEDTECH (SHENZHEN) CO.,LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Jun 15, 2026
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 80898209025 and manufactured by HIWIN MEDTECH (SHENZHEN) CO.,LTD.. The registration is held by LAIBO MEDICAL PRODUTOS MEDICOS E 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.