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CORONAVIRUS - ANVISA Registration 10071770932

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 10071770932 and manufactured by manufacturer not specified. The registration is held by ABBOTT DIAGNOSTICOS RAPIDOS S.A. with validity until Sep 19, 2032.

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.

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10071770932
2 Related Devices
Registration Details
ANVISA Registration Number: 10071770932
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Related Devices (2)

Família ID NOW COVID-19 2.0
Risk Class III

Registration Details

10071770932

25351145055202211

50248780000161

Company Information

Dates and Status

Sep 19, 2022

19/09/2032

09/18/2025 19:00:01

Família ID NOW COVID-19 2.0
Risk Class III

Registration Details

10071770932

25351145055202211

50248780000161

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Sep 19, 2022

19/09/2032

09/18/2025 19:00:01