Ureteroscope - ANVISA Registration 80459130062

Access comprehensive regulatory information for Ureteroscope in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80459130062 and manufactured by MAXIFLEX, LLC. The registration is held by MEDICAL BRAZIL IMPORTAÇÃO, EXPORTAÇÃO E COMÉRCIO DE PRODUTOS MÉDICOS 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 E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME, SHENZHEN HUGEMED MEDICAL TECHNICAL DEVELOPMENT 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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80459130062
Registration Details
ANVISA Registration Number: 80459130062
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

Flex XI U
Risk Class II

Registration Details

80459130062

25351273600201873

09423516000113

Company Information

MAXIFLEX, LLC
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jun 25, 2018

VIGENTE

09/18/2025 19:00:01