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FERTILITY SELF-TEST - ANVISA Registration 10163770009

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 10163770009 and manufactured by GUANG ZHOU WONDFO BIOTECH CO. LTDA. The registration is held by BLAU FARMACEUTICA S.A. 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 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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10163770009
Registration Details
ANVISA Registration Number: 10163770009
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Device Details

FERTILITY DAY TESTE DE OVULAÇÃO
Risk Class II

Registration Details

10163770009

250000254739864

58430828000160

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Oct 22, 1998

VIGENTE

09/18/2025 19:00:01