CORONAVIRUS - ANVISA Registration 80022230230
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 80022230230 and manufactured by GOLD ANALISA DIAGNOSTICA LTDA. The registration is held by GOLD ANALISA DIAGNOSTICA LTDA with validity until May 24, 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
80022230230
25351400668202137
03142794000116
Company Information
Dates and Status
May 24, 2021
24/05/2031
09/18/2025 19:00:01
CORONAVIRUS
Covid Ag Oral ECO Detect
Eco Diagnostica Ltda
80954880149
Oct 01, 2020
CORONAVIRUS
Covid-19 Ag Rapid Test (Oral Fluid)
LABTEST DIAGNOSTICA S/A
10009010371
May 31, 2021
CORONAVIRUS
TESTE RÁPIDO AG ORAL COVID-19
Not specified
81325990167
Mar 15, 2021
CORONAVIRUS
TESTE RÁPIDO AG ORAL COVID-19
ACRO BIOTECH, INC. (MONTCLAIR)
81325990167
Mar 15, 2021
CORONAVIRUS
COVID-19 Ag
IN VITRO DIAGNOSTICA LTDA
10303460509
Aug 02, 2021
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