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CORONAVIRUS - ANVISA Registration 10360810062

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 10360810062 and manufactured by manufacturer not specified. The registration is held by DOC MED COMERCIO IMPORTACAO E EXPORTACAO LTDA with validity until Jun 14, 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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10360810062
2 Related Devices
Registration Details
ANVISA Registration Number: 10360810062
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Related Devices (2)

FAMÍLIA MERIL TESTE RÁPIDO COVID-19 ONE STEP RT-PCR
Risk Class III

Registration Details

10360810062

25351667241202036

66877184000180

Company Information

Dates and Status

Jun 14, 2021

14/06/2031

09/18/2025 19:00:01

FAMÍLIA MERIL TESTE RÁPIDO COVID-19 ONE STEP RT-PCR
Risk Class III

Registration Details

10360810062

25351667241202036

66877184000180

Company Information

India
PT: ÍNDIA

Dates and Status

Jun 14, 2021

14/06/2031

09/18/2025 19:00:01