LUTEINIZING HORMONE (LH) - ANVISA Registration 81298810081

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 81298810081 and manufactured by TOSOH CORPORATION. The registration is held by MD CONSULTORIA E COMERCIO DE PRODUTOS PARA LABORATORIO LTDA - ME 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 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Similar Products
5 Competitors
81298810081
Registration Details
ANVISA Registration Number: 81298810081
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

🇧🇷 Brazil Regulatory Expert

Need help with your Brazil registration?

Contact Pure Global Brazil Team
Free consultation

Device Details

Família de Reagente e Calibradores ST AIA-PACK LH II (Hormônio Luteinizante)
Risk Class II

Registration Details

81298810081

25351208776201902

23000972000181

Company Information

TOSOH CORPORATION
Japan
PT: JAPÃO

Dates and Status

Jul 01, 2019

VIGENTE

09/18/2025 19:00:01