CORONAVIRUS - ANVISA Registration 81077790014
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 81077790014 and manufactured by REM INDUSTRIA E COMERCIO SOCIEDADE UNIPESSOAL LTDA. The registration is held by REM INDUSTRIA E COMERCIO SOCIEDADE UNIPESSOAL LTDA with validity until Jun 10, 2030.
This page provides complete technical specifications for this device, regulatory compliance details, 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.
Device Details
Registration Details
81077790014
25351416013202008
47334701000635
Company Information
Dates and Status
Jun 10, 2020
10/06/2030
09/18/2025 19:00:01
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

