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CORONAVIRUS - ANVISA Registration 10033121018

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 10033121018 and manufactured by manufacturer not specified. The registration is held by BECKMAN COULTER DO BRASIL COMÉRCIO E IMPORTAÇÃO DE PRODUTOS DE LABORATÓRIO LTDA with validity until Apr 19, 2031.

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.

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10033121018
2 Related Devices
Registration Details
ANVISA Registration Number: 10033121018
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Related Devices (2)

Família de Reagente, Calibrador e Controle Access SARS-Cov-2 IgG II
Risk Class III

Registration Details

10033121018

25351087209202153

42160812000144

Dates and Status

Apr 19, 2021

19/04/2031

09/18/2025 19:00:01

Família de Reagente, Calibrador e Controle Access SARS-Cov-2 IgG II
Risk Class III

Registration Details

10033121018

25351087209202153

42160812000144

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Apr 19, 2021

19/04/2031

09/18/2025 19:00:01