SELF-TEST FOR HUMAN CHORIONIC GONADOTROPIN (HCG) - ANVISA Registration 10310030146

Access comprehensive regulatory information for SELF-TEST FOR HUMAN CHORIONIC GONADOTROPIN (HCG) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10310030146 and manufactured by WAMA PRODUTOS PARA LABORATORIO LTDA. The registration is held by WAMA PRODUTOS PARA LABORATORIO 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
10310030146
Registration Details
ANVISA Registration Number: 10310030146
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

Registration Details

10310030146

25351667021201238

66000787000108

Company Information

Brazil
PT: BRASIL

Dates and Status

Jan 21, 2013

VIGENTE

09/18/2025 19:00:01