Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

SELF-TEST FOR FOLLICLE STIMULATING HORMONE (FSH) - ANVISA Registration 81325990209

Access comprehensive regulatory information for SELF-TEST 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 81325990209 and manufactured by HANGZHOU ALLTEST BIOTECH CO. LTD. The registration is held by QR CONSULTING, IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS 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 ACRO BIOTECH, INC. (MONTCLAIR), SEJOY BIOMEDICAL CO., LTD., 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 Competitors
5 Recent Registrations
81325990209
Registration Details
ANVISA Registration Number: 81325990209
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Família Teste Rápido de FSH (Urina-Jato médio) para Autoteste (FFS-103H) (Midstream)
Risk Class II

Registration Details

81325990209

25351607687202273

19933144000129

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jan 09, 2023

VIGENTE

09/18/2025 19:00:01