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FOLLICLE STIMULATING HORMONE (FSH) - ANVISA Registration 82444370267

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 82444370267 and manufactured by ZHEJIANG ORIENT GENE BIOTECH CO., LTD.. The registration is held by Enzytec Biotecnologia 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 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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82444370267
Registration Details
ANVISA Registration Number: 82444370267
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Device Details

Família FSH Quantitative Test Kit (Time-Resolved FIA)
Risk Class II

Registration Details

82444370267

25351124464202518

07214566000165

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Sep 08, 2025

VIGENTE

09/18/2025 19:00:01