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ANVISA registration 81576620002Active

CORONARY ANGIOPLASTY BALLOON CATHETER

ANVISA Registration Number: 81576620002CORDIS MEDICAL BRASIL LTDAKANEKA CORPORATIONRisk Class IV
Verified
Device names
Technical name
CORONARY ANGIOPLASTY BALLOON CATHETER
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PT: CATETER BALÃO PARA ANGIOPLASTIA CORONÁRIA
Commercial name
Catéter Balão Kaneka PTCA
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Risk class
Class IV
Registration details
Registration Number
81576620002
Process Number
25351102619202301
CNPJ
27548227000122
Company information
Registration Holder
CORDIS MEDICAL BRASIL LTDA
Manufacturer
KANEKA CORPORATION
Manufacturing Country
Japan
PT: JAPÃO
Dates and status
Publication Date
Mar 06, 2023
Status
Active
About this record

Access comprehensive regulatory information for CORONARY ANGIOPLASTY BALLOON CATHETER in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 81576620002 and manufactured by KANEKA CORPORATION. The registration is held by CORDIS MEDICAL BRASIL LTDA with validity until Aug 05, 2029.

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.