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ANVISA registration 81576620010Valid until Apr 14, 2028

PERIPHERAL ANGIOPLASTY BALLOON CATHETER

ANVISA Registration Number: 81576620010CORDIS MEDICAL BRASIL LTDACLEARSTREAM TECHNOLOGIES LTDRisk Class III
Verified
Device names
Technical name
PERIPHERAL ANGIOPLASTY BALLOON CATHETER
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PT: CATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA
Commercial name
CATETER PERIFERICO PARA ANGIOPLASTIA TRANSLUMINAL PERCUTÂNEA (PTA) SAVVY*LONG
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Risk class
Class III
Registration details
Registration Number
81576620010
Process Number
25351102788202333
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
14/04/2028
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 III medical device is registered under ANVISA number 81576620010 and manufactured by CLEARSTREAM TECHNOLOGIES LTD. The registration is held by CORDIS MEDICAL BRASIL LTDA with validity until Apr 14, 2028.

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.