CORONAVIRUS - ANVISA Registration 80638720174
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 80638720174 and manufactured by DIAGNÓSTICA INDÚSTRIA E COMÉRCIO LTDA - ME. The registration is held by DIAGNÓSTICA INDÚSTRIA E COMÉRCIO LTDA - ME with validity until Mar 22, 2031.
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
80638720174
25351088052202183
11462456000190
Company Information
Dates and Status
Mar 22, 2021
22/03/2031
09/18/2025 19:00:01
CORONAVIRUS
COVID 19 AG TEST
Not specified
80027310291
Dec 07, 2020
CORONAVIRUS
COVID 19 AG TEST
BEIJING LEPU MEDICAL TECHNOLOGY CO., LTD.
80027310291
Dec 07, 2020
CORONAVIRUS
COVID-19 Ag Test
BEIJING CORE TECHNOLOGY CO., LTD.
80882270007
Mar 14, 2022
CORONAVIRUS
COVID-19 Ag Test
Not specified
80882270007
Mar 14, 2022
CORONAVIRUS
COVID-19 AG RAPID TEST
GUANGZHOU WONDFO BIOTECH CO.LTD
80638720170
Dec 14, 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