CORONAVIRUS - ANVISA Registration 10230730138

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 10230730138 and manufactured by manufacturer not specified. The registration is held by NL COMÉRCIO EXTERIOR LTDA with validity until Nov 30, 2030.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 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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10230730138
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Registration Details
ANVISA Registration Number: 10230730138
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Família SARS-CoV-2 Antigen Rapid Test
Risk Class III

Registration Details

10230730138

25351423382202049

52541273000147

Company Information

Dates and Status

Nov 30, 2020

30/11/2030

09/18/2025 19:00:01

Família SARS-CoV-2 Antigen Rapid Test
Risk Class III

Registration Details

10230730138

25351423382202049

52541273000147

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Nov 30, 2020

30/11/2030

09/18/2025 19:00:01