CORONAVIRUS - ANVISA Registration 81325990179

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 81325990179 and manufactured by manufacturer not specified. The registration is held by QR CONSULTING, IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS LTDA with validity until May 03, 2031.

This page provides complete technical specifications for 2 related devices, 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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81325990179
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Registration Details
ANVISA Registration Number: 81325990179
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Teste Rápido de Antígeno COVID-19 – ACRO LF
Risk Class III

Registration Details

81325990179

25351143707202193

19933144000129

Dates and Status

May 03, 2021

03/05/2031

09/18/2025 19:00:01

Teste Rápido de Antígeno COVID-19 – ACRO LF
Risk Class III

Registration Details

81325990179

25351143707202193

19933144000129

Company Information

ACRO BIOTECH INC
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

May 03, 2021

03/05/2031

09/18/2025 19:00:01