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CORONAVIRUS - ANVISA Registration 80020690408

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 80020690408 and manufactured by manufacturer not specified. The registration is held by BIO-RAD LABORATORIOS BRASIL LTDA with validity until Aug 03, 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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80020690408
2 Related Devices
Registration Details
ANVISA Registration Number: 80020690408
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Related Devices (2)

Platelia SARS-CoV-2 Total Ab
Risk Class III

Registration Details

80020690408

25351376801202046

03188198000177

Company Information

Dates and Status

Aug 03, 2020

03/08/2030

09/18/2025 19:00:01

Platelia SARS-CoV-2 Total Ab
Risk Class III

Registration Details

80020690408

25351376801202046

03188198000177

Company Information

BIO-RAD
France
PT: FRANÇA

Dates and Status

Aug 03, 2020

03/08/2030

09/18/2025 19:00:01