CORONAVIRUS - ANVISA Registration 10009010361
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 10009010361 and manufactured by LABTEST DIAGNOSTICA S/A. The registration is held by LABTEST DIAGNOSTICA S/A with validity until Sep 24, 2030.
This page provides complete technical specifications for this device, 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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Registration Details
10009010361
25351974475202037
16516296000138
Company Information
Dates and Status
Sep 24, 2020
24/09/2030
09/18/2025 19:00:01
CORONAVIRUS
COVID-19 AG RAPID TEST
Not specified
80638720170
Dec 14, 2020
CORONAVIRUS
COVID-19 AG RAPID TEST
DIAGNÓSTICA INDÚSTRIA E COMÉRCIO LTDA - ME
80638720181
Jun 14, 2021
CORONAVIRUS
COVID-19 AG RAPID TEST
GUANGZHOU WONDFO BIOTECH CO.LTD
80638720170
Dec 14, 2020
CORONAVIRUS
COVID-19 AG RAPID TEST
HUMASIS CO., LTD
80638720162
Sep 10, 2020
CORONAVIRUS
COVID-19 AG RAPID TEST
Not specified
80638720162
Sep 10, 2020
CORONAVÍRUS
Kit Rápido de Detecção de Antígeno de SARS-CoV-2 (COVID-19)
JIANGSU BIOPERFECTUS TECHNOLOGIES CO., LTD.
82444370255
Sep 01, 2025
CORONAVÍRUS
Kit Rápido de Detecção de Antígeno de SARS-CoV-2 (COVID-19)
Not specified
82444370255
Sep 01, 2025
CORONAVÍRUS
Teste Rápido COVID-19
Not specified
81472060050
Aug 25, 2025
CORONAVÍRUS
Teste Rápido COVID-19
HANGZHOU AICHEK MEDICAL TECHNOLOGY CO., LTD.
81472060050
Aug 25, 2025
CORONAVÍRUS
Xpert Xpress CoV-2 plus
Not specified
81062710058
Aug 18, 2025