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CORONAVIRUS - ANVISA Registration 80146502251

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 80146502251 and manufactured by ABBOTT MOLECULAR INC.. The registration is held by ABBOTT LABORATORIOS DO BRASIL LTDA with validity until May 11, 2030.

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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80146502251
2 Related Devices
Registration Details
ANVISA Registration Number: 80146502251
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Related Devices (2)

Família Abbott RealTime SARS-CoV-2
Risk Class III

Registration Details

80146502251

25351317561202048

56998701000116

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

May 11, 2020

11/05/2030

09/18/2025 19:00:01

Família Abbott RealTime SARS-CoV-2
Risk Class III

Registration Details

80146502251

25351317561202048

56998701000116

Company Information

Dates and Status

May 11, 2020

11/05/2030

09/18/2025 19:00:01