FOLLICLE STIMULATING HORMONE (FSH) - ANVISA Registration 80102513112

Access comprehensive regulatory information for FOLLICLE STIMULATING HORMONE (FSH) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80102513112 and manufactured by AUTOBIO DIAGNOSTICS CO., LTD. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS 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 ABBOTT IRELAND DIAGNOSTICS DIVISION, ROCHE DIAGNOSTICS GMBH, 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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80102513112
Registration Details
ANVISA Registration Number: 80102513112
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

Família AutoLumo FSH Micropartículas (CLIA)
Risk Class II

Registration Details

80102513112

25351628762202311

04718143000194

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Oct 30, 2023

VIGENTE

09/18/2025 19:00:01