CORONAVIRUS - ANVISA Registration 80049120112

Access comprehensive regulatory information for CORONAVIRUS in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80049120112 and manufactured by ALAMAR TECNO CIENTÍFICA LTDA. The registration is held by ALAMAR TECNO CIENTÍFICA LTDA with validity until May 03, 2031.

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 GUANGZHOU WONDFO BIOTECH CO., LTD., Eco Diagnostica 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
80049120112
Registration Details
ANVISA Registration Number: 80049120112
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

ANTÍGENO SARS-CoV-2 SALIVA TESTE RÁPIDO
Risk Class III

Registration Details

80049120112

25351306222202117

48044358000142

Company Information

Brazil
PT: BRASIL

Dates and Status

May 03, 2021

03/05/2031

09/18/2025 19:00:01