Pure Global AI
ANVISA registration 81576620015Valid until May 05, 2028

PERIPHERAL ANGIOPLASTY BALLOON CATHETER

ANVISA Registration Number: 81576620015CORDIS MEDICAL BRASIL LTDACLEARSTREAM TECHNOLOGIES LTDRisk Class III
Verified
Device names
Technical name
PERIPHERAL ANGIOPLASTY BALLOON CATHETER
View exact technical-name matches →
PT: CATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA
Commercial name
CATETER PARA ANGIOPLASTIA TRANSLUMINAL PERCUTANEO (PTA) SLEEK
View exact commercial-name matches →
Risk class
Class III
Registration details
Registration Number
81576620015
Process Number
25351102953202357
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
05/05/2028
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 81576620015 and manufactured by CLEARSTREAM TECHNOLOGIES LTD. The registration is held by CORDIS MEDICAL BRASIL LTDA with validity until May 05, 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.