FERTILITY SELF-TEST - ANVISA Registration 82948680002

Access comprehensive regulatory information for FERTILITY SELF-TEST in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82948680002 and manufactured by HANGZHOU ALLTEST BIOTECH 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 similar products found using AI-powered semantic search, 5 companies making the same product including HANGZHOU ALLTEST BIOTECH CO. LTD, ALAMAR TECNO CIENTÍFICA LTDA, 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
82948680002
Registration Details
ANVISA Registration Number: 82948680002
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

Famivita Fertilidade Masculina
Risk Class II

Registration Details

82948680002

25351135924202533

23583042000289

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Sep 15, 2025

VIGENTE

09/18/2025 19:00:01