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CORONAVIRUS - ANVISA Registration 10361530018

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 10361530018 and manufactured by manufacturer not specified. The registration is held by DATAMED LTDA with validity until Nov 12, 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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10361530018
2 Related Devices
Registration Details
ANVISA Registration Number: 10361530018
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Related Devices (2)

Real-time fluorescent RT-PCR kit for detecting 2019-nCoV
Risk Class III

Registration Details

10361530018

25351528713202036

38658399000175

Company Information

Dates and Status

Nov 12, 2020

12/11/2030

09/18/2025 19:00:01

Real-time fluorescent RT-PCR kit for detecting 2019-nCoV
Risk Class III

Registration Details

10361530018

25351528713202036

38658399000175

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Nov 12, 2020

12/11/2030

09/18/2025 19:00:01