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SELF-TEST FOR FOLLICLE STIMULATING HORMONE (FSH) - ANVISA Registration 80113770046

Access comprehensive regulatory information for SELF-TEST 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 80113770046 and manufactured by HANGZHOU ALLTEST 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 companies making the same product including ACRO BIOTECH, INC. (MONTCLAIR), SEJOY BIOMEDICAL 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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80113770046
Registration Details
ANVISA Registration Number: 80113770046
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Device Details

Família Autoteste de Menopausa (Midstream) (Apresentação com 1 teste)
Risk Class II

Registration Details

80113770046

25351303420202471

03098281000155

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jun 17, 2024

VIGENTE

09/18/2025 19:00:01