VAGINAL PH SELF-TEST - ANVISA Registration 80113770052
Access comprehensive regulatory information for VAGINAL PH SELF-TEST in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80113770052 and manufactured by ZHEJIANG ORIENT GENE 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, 1 companies making the same product including CHEMBIO DIAGNOSTICS BRAZIL LTDA., and 1 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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Registration Details
80113770052
25351403565202471
03098281000155
Company Information
Dates and Status
Dec 23, 2024
VIGENTE
09/18/2025 19:00:01
VAGINAL PH SELF-TEST
Autoteste de pH feminino - Exacto
CHEMBIO DIAGNOSTICS BRAZIL LTDA.
80535240074
Feb 17, 2025
FERTILITY SELF-TEST
FAMILIA AUTOTESTE DE FERTILIDADE
SANFARMA INDÚSTRIA, COMÉRCIO, IMPORTAÇÃO E EXPORTAÇÃO LTDA
80015040051
Jul 08, 2024
FERTILITY SELF-TEST
Família Teste de Ovulação
HANGZHOU AICHEK MEDICAL TECHNOLOGY CO., LTD.
82444370093
Feb 19, 2024
FERTILITY SELF-TEST
Família Autoteste de Fertilidade 30
HANGZHOU ALLTEST BIOTECH CO. LTD
80113770047
Aug 05, 2024
SELF-TEST FOR FOLLICLE STIMULATING HORMONE (FSH)
Família Autoteste de Menopausa (Midstream) (Apresentação com 1 teste)
HANGZHOU ALLTEST BIOTECH CO. LTD
80113770046
Jun 17, 2024