PERIPHERAL ANGIOPLASTY BALLOON CATHETER - ANVISA Registration 80174309029

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 80174309029 and manufactured by YILSON MEDICAL TECHNOLOGY CO., LTD.. The registration is held by VALFLUX COMERCIO DE MATERIAIS HOSPITALARES 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Similar Products
5 Competitors
80174309029
Registration Details
ANVISA Registration Number: 80174309029
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

Registration Details

80174309029

25351060801202531

03872497000126

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

May 05, 2025

VIGENTE

09/18/2025 19:00:01