Pure Global

Dilatation Balloons - ANVISA Registration 81522530002

Access comprehensive regulatory information for Dilatation Balloons in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81522530002 and manufactured by TAE YEON MEDICAL CO., LTD. The registration is held by MIVIDA ASSUNTOS REGULATORIOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including E-MED PRODUTOS Mร‰DICO-HOSPITALARES LTDA - ME, MEDTEC SUPPLIES, INDUSTRIA, IMPORTACAO, EXPORTACAO, DISTRIBUICAO E COMERCIO LTDA, 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 Competitors
5 Recent Registrations
81522530002
Registration Details
ANVISA Registration Number: 81522530002
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Cateter - Balรฃo para Cifoplastia
Risk Class I

Registration Details

81522530002

25351453350202400

25263704000188

Company Information

South Korea
PT: CORร‰IA DO SUL

Dates and Status

Dec 23, 2024

VIGENTE

09/18/2025 19:00:01