CORONAVIRUS - ANVISA Registration 10345162410

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 10345162410 and manufactured by manufacturer not specified. The registration is held by SIEMENS HEALTHCARE DIAGNÓSTICOS LTDA with validity until Sep 13, 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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10345162410
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Registration Details
ANVISA Registration Number: 10345162410
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

CLINITEST Rapid COVID-19 Antigen Test
Risk Class III

Registration Details

10345162410

25351753371202171

01449930000190

Company Information

Dates and Status

Sep 13, 2021

13/09/2031

09/18/2025 19:00:01

CLINITEST Rapid COVID-19 Antigen Test
Risk Class III

Registration Details

10345162410

25351753371202171

01449930000190

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Sep 13, 2021

13/09/2031

09/18/2025 19:00:01