Pure Global

CORONAVIRUS - ANVISA Registration 81984510003

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 81984510003 and manufactured by manufacturer not specified. The registration is held by Key Trade Importadora e Exportadora Ltda with validity until Mar 22, 2031.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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 Competitors
5 Recent Registrations
81984510003
2 Related Devices
Registration Details
ANVISA Registration Number: 81984510003
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Related Devices (2)

Teste de Antígeno Artron para COVID-19
Risk Class III

Registration Details

81984510003

25351023240202166

09211470000179

Company Information

Dates and Status

Mar 22, 2021

22/03/2031

09/18/2025 19:00:01

Teste de Antígeno Artron para COVID-19
Risk Class III

Registration Details

81984510003

25351023240202166

09211470000179

Company Information

Canada
PT: CANADÁ

Dates and Status

Mar 22, 2021

22/03/2031

09/18/2025 19:00:01