CORONAVIRUS - ANVISA Registration 80680420089
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 80680420089 and manufactured by MICO BIOMED CO.,LTD.. The registration is held by BIO BRASIL BIOTECNOLOGIA LTDA with validity until Sep 04, 2033.
This page provides complete technical specifications for 2 related devices, 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.
Related Devices (2)
Registration Details
80680420089
25351027830202320
10942372000190
Company Information
Dates and Status
Sep 04, 2023
04/09/2033
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

