CORONAVIRUS - ANVISA Registration 80102512693

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 80102512693 and manufactured by SEEGENE INC.. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Aug 23, 2031.

This page provides complete technical specifications for 2 related devices, 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
80102512693
2 Related Devices
Registration Details
ANVISA Registration Number: 80102512693
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

Related Devices (2)

Allplex™ SARS-CoV-2 Master Assay
Risk Class III

Registration Details

80102512693

25351383164202145

04718143000194

Company Information

SEEGENE INC.
South Korea
PT: CORÉIA DO SUL

Dates and Status

Aug 23, 2021

23/08/2031

09/18/2025 19:00:01

Allplex™ SARS-CoV-2 Master Assay
Risk Class III

Registration Details

80102512693

25351383164202145

04718143000194

Dates and Status

Aug 23, 2021

23/08/2031

09/18/2025 19:00:01