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CORONAVIRUS - ANVISA Registration 81425780025

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 81425780025 and manufactured by manufacturer not specified. The registration is held by OLTRAMED COMERCIO DE PRODUTOS MEDICOS LTDA - EPP with validity until Apr 20, 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.

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81425780025
2 Related Devices
Registration Details
ANVISA Registration Number: 81425780025
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Related Devices (2)

Diagnostic Kit for IgM/IgG Antibody to Coronavirus (SAR S-CoV-2) (Lateral Flow)
Risk Class III

Registration Details

81425780025

25351235560202086

14829987000166

Company Information

Dates and Status

Apr 20, 2020

20/04/2030

09/18/2025 19:00:01

Diagnostic Kit for IgM/IgG Antibody to Coronavirus (SAR S-CoV-2) (Lateral Flow)
Risk Class III

Registration Details

81425780025

25351235560202086

14829987000166

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Apr 20, 2020

20/04/2030

09/18/2025 19:00:01