CORONAVIRUS - ANVISA Registration 10287411536

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 10287411536 and manufactured by manufacturer not specified. The registration is held by ROCHE DIAGNÓSTICA BRASIL LTDA with validity until Oct 01, 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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10287411536
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Registration Details
ANVISA Registration Number: 10287411536
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

SARS-CoV-2 Rapid Antigen Test
Risk Class III

Registration Details

10287411536

25351958261202013

30280358000186

Company Information

Dates and Status

Oct 01, 2020

01/10/2030

09/18/2025 19:00:01

SARS-CoV-2 Rapid Antigen Test
Risk Class III

Registration Details

10287411536

25351958261202013

30280358000186

Company Information

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

Dates and Status

Oct 01, 2020

01/10/2030

09/18/2025 19:00:01