PERIPHERAL ANGIOPLASTY BALLOON CATHETER - ANVISA Registration 80312279058

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 80312279058 and manufactured by BIOTRONIK AG. The registration is held by TELEFLEX MEDICAL BRASIL 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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80312279058
Registration Details
ANVISA Registration Number: 80312279058
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

Catéter Balão pra Angioplastia Periférica - PASSEO-35 XEO
Risk Class II

Registration Details

80312279058

25351155375202513

06089071000199

Company Information

BIOTRONIK AG
Switzerland
PT: SUÍÇA

Dates and Status

Sep 15, 2025

VIGENTE

09/18/2025 19:00:01