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CORONAVIRUS - ANVISA Registration 10330660323

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 10330660323 and manufactured by manufacturer not specified. The registration is held by DESCARPACK DESCARTAVEIS DO BRASIL LTDA with validity until Nov 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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10330660323
2 Related Devices
Registration Details
ANVISA Registration Number: 10330660323
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Related Devices (2)

Teste Rápido Standard Q COVID-19 IgM/IgG COMBO
Risk Class III

Registration Details

10330660323

25351603875202061

01057428000133

Company Information

Dates and Status

Nov 03, 2020

03/11/2030

09/18/2025 19:00:01

Teste Rápido Standard Q COVID-19 IgM/IgG COMBO
Risk Class III

Registration Details

10330660323

25351603875202061

01057428000133

Company Information

SD BIOSENSOR, INC.
South Korea
PT: CORÉIA DO SUL

Dates and Status

Nov 03, 2020

03/11/2030

09/18/2025 19:00:01