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ANVISA registration 81576629022Active

PERIPHERAL ANGIOPLASTY BALLOON CATHETER

ANVISA Registration Number: 81576629022CORDIS MEDICAL BRASIL LTDACORDIS US CORP.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 PARA ANGIOPLASTIA TRANSLUMINAL PERCUTÂNEA (PTA) SABERX™ 0.014
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Risk class
Class II
Registration details
Registration Number
81576629022
Process Number
25351794695202321
CNPJ
27548227000122
Company information
Registration Holder
CORDIS MEDICAL BRASIL LTDA
Manufacturer
CORDIS US CORP.
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Dec 11, 2023
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 81576629022 and manufactured by CORDIS US CORP.. The registration is held by CORDIS MEDICAL BRASIL 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.