FERTILITY SELF-TEST - ANVISA Registration 82195300012

Access comprehensive regulatory information for FERTILITY 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 82195300012 and manufactured by ACMEX BIO-TECHNOLOGY (CHONGQING) CO., LTD.. The registration is held by PURE LATAM BRAZIL COMERCIO DE PRODUTOS HOSPITALARES 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 HANGZHOU ALLTEST BIOTECH CO. LTD, ALAMAR TECNO CIENTÍFICA 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.

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82195300012
Registration Details
ANVISA Registration Number: 82195300012
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

Teste rápido de ovulação (LH)
Risk Class II

Registration Details

82195300012

25351423602202468

27939884000109

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jan 13, 2025

VIGENTE

09/18/2025 19:00:01