FOLLICLE STIMULATING HORMONE (FSH) - ANVISA Registration 80113770054

Access comprehensive regulatory information for FOLLICLE STIMULATING HORMONE (FSH) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80113770054 and manufactured by GUANGZHOU WONDFO BIOTECH CO. LTD. The registration is held by ALEXDAN IMPORTAÇÃO E EXPORTAÇÃO LTDA – EPP 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 ABBOTT IRELAND DIAGNOSTICS DIVISION, ROCHE DIAGNOSTICS GMBH, 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
80113770054
Registration Details
ANVISA Registration Number: 80113770054
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

Família Autoteste de Menopausa em Tira
Risk Class II

Registration Details

80113770054

25351142780202571

03098281000155

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Sep 15, 2025

VIGENTE

09/18/2025 19:00:01