PERIPHERAL ANGIOPLASTY BALLOON CATHETER - ANVISA Registration 80224390214

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 80224390214 and manufactured by Creagh Medical Ltd. The registration is held by BIOTRONIK COMERCIAL MÉDICA LTDA. with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including BOSTON SCIENTIFIC CORPORATION, BROSMED MEDICAL CO., LTD, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.

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80224390214
Registration Details
ANVISA Registration Number: 80224390214
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

CATETER BALÃO PARA DILATAÇÃO PERIFÉRICA DE ALTA PRESSÃO PASSEO-35 HP
Risk Class II

Registration Details

80224390214

25351543377201311

50595271000105

Company Information

Creagh Medical Ltd
Ireland
PT: IRLANDA

Dates and Status

Apr 28, 2014

VIGENTE

09/18/2025 19:00:01