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ANVISA registration 81576620028Valid until Jan 30, 2027

PERIPHERAL ANGIOPLASTY BALLOON CATHETER

ANVISA Registration Number: 81576620028CORDIS MEDICAL BRASIL LTDACLEARSTREAM TECHNOLOGIES LTDRisk Class IV
Verified
Device names
Technical name
PERIPHERAL ANGIOPLASTY BALLOON CATHETER
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PT: CATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA
Commercial name
CATETER PARA ANGIOPLASTIA TRANSLUMINAL PERCUTÂNEA SLEEK OTW
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Risk class
Class IV
Registration details
Registration Number
81576620028
Process Number
25351103488202371
CNPJ
27548227000122
Company information
Registration Holder
CORDIS MEDICAL BRASIL LTDA
Manufacturer
CLEARSTREAM TECHNOLOGIES LTD
Manufacturing Country
Ireland
PT: IRLANDA
Dates and status
Publication Date
Mar 06, 2023
Validity
30/01/2027
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 IV medical device is registered under ANVISA number 81576620028 and manufactured by CLEARSTREAM TECHNOLOGIES LTD. The registration is held by CORDIS MEDICAL BRASIL LTDA with validity until Jan 30, 2027.

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.