CORONAVIRUS - ANVISA Registration 10287411671

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 10287411671 and manufactured by manufacturer not specified. The registration is held by ROCHE DIAGNÓSTICA BRASIL LTDA with validity until Aug 21, 2033.

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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10287411671
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Registration Details
ANVISA Registration Number: 10287411671
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

SARS-CoV-2 Rapid Antigen Test 2.0
Risk Class III

Registration Details

10287411671

25351247527202341

30280358000186

Company Information

Dates and Status

Aug 21, 2023

21/08/2033

09/18/2025 19:00:01

SARS-CoV-2 Rapid Antigen Test 2.0
Risk Class III

Registration Details

10287411671

25351247527202341

30280358000186

Company Information

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

Dates and Status

Aug 21, 2023

21/08/2033

09/18/2025 19:00:01