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SELF-TEST FOR SARS-COV-2 ANTIGEN (CORONAVIRUS) - ANVISA Registration 81203440014

Access comprehensive regulatory information for SELF-TEST FOR SARS-COV-2 ANTIGEN (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 81203440014 and manufactured by manufacturer not specified. The registration is held by BIOTECH LOGÍSTICA LTDA- EPP with validity until Apr 17, 2033.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including HANGZHOU ALLTEST BIOTECH CO. LTD, GENRUI BIOTECH INC., 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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81203440014
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Registration Details
ANVISA Registration Number: 81203440014
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Related Devices (2)

COVI-Pro™ Autoteste rápido de antígeno COVID-19
Risk Class III

Registration Details

81203440014

25351265920202236

21382943000104

Company Information

Dates and Status

Apr 17, 2023

17/04/2033

09/18/2025 19:00:01

COVI-Pro™ Autoteste rápido de antígeno COVID-19
Risk Class III

Registration Details

81203440014

25351265920202236

21382943000104

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Apr 17, 2023

17/04/2033

09/18/2025 19:00:01