CORONARY ANGIOPLASTY BALLOON CATHETER - ANVISA Registration 80224390318

Access comprehensive regulatory information for CORONARY 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 80224390318 and manufactured by BIOTRONIK COMERCIAL MÉDICA LTDA.. The registration is held by BIOTRONIK COMERCIAL MÉDICA LTDA. with validity until Jun 30, 2035.

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 LEPU MEDICAL TECHNOLOGY (BEIJING) CO., LTD, BOSTON SCIENTIFIC CORPORATION - MARLBOROUGH, 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Similar Products
5 Competitors
80224390318
Registration Details
ANVISA Registration Number: 80224390318
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

🇧🇷 Brazil Regulatory Expert

Need help with your Brazil registration?

Contact Pure Global Brazil Team
Free consultation

Device Details

TrapIT - CATETER BALÃO PARA APRISIONAMENTO DE FIO GUIA CORONARIANO
Risk Class III

Registration Details

80224390318

25351410687202414

50595271000105

Company Information

Brazil
PT: BRASIL

Dates and Status

Jun 30, 2025

30/06/2035

09/18/2025 19:00:01