CORONAVIRUS - ANVISA Registration 80859840202
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 80859840202 and manufactured by SHANGAI BIOGERM MEDICAL TECHNOLOGY., LTD. LOCALIZADA. The registration is held by CPMH - Comércio e Indústria de Produtos Médico-Hospitalares e Odontológicos LTDA. with validity until Apr 27, 2030.
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
80859840202
25351223955202036
13532259000125
Company Information
Dates and Status
Apr 27, 2020
27/04/2030
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

