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LUTEINIZING HORMONE (LH) - ANVISA Registration 82948680001

Access comprehensive regulatory information for LUTEINIZING HORMONE (LH) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82948680001 and manufactured by INNOVITA (TANGSHAN) BIOLOGICAL TECHNOLOGY CO., LTD.. The registration is held by famivita comércio de produtos para saúde ltda. 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 ROCHE DIAGNOSTICS GMBH, ABBOTT IRELAND DIAGNOSTICS DIVISION, 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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82948680001
Registration Details
ANVISA Registration Number: 82948680001
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Device Details

Teste de Ovulação Famivita
Risk Class II

Registration Details

82948680001

25351116790202551

23583042000289

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Sep 01, 2025

VIGENTE

09/18/2025 19:00:01