CORONAVIRUS - ANVISA Registration 82036180016

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 82036180016 and manufactured by XIAMEN BOSON BIOTECH CO., LTD. The registration is held by CONNECT ASSUNTOS REGULATÓRIOS, COMÉRCIO E DISTRIBUIDORA DE PRODUTOS MÉDICO-HOSPITALRES LTDA with validity until Jan 25, 2031.

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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82036180016
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Registration Details
ANVISA Registration Number: 82036180016
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

RAPID SARS-COV-2 ANTIGEN TEST CARD
Risk Class III

Registration Details

82036180016

25351278179202010

37026700000165

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jan 25, 2021

25/01/2031

09/18/2025 19:00:01

RAPID SARS-COV-2 ANTIGEN TEST CARD
Risk Class III

Registration Details

82036180016

25351278179202010

37026700000165

Dates and Status

Jan 25, 2021

25/01/2031

09/18/2025 19:00:01