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CORONAVIRUS - ANVISA Registration 80844240002

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 80844240002 and manufactured by PANTEST SA. The registration is held by BIOFAC INDUSTRIA, COMERCIO E REPRESENTACAO LTDA with validity until Dec 07, 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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80844240002
2 Related Devices
Registration Details
ANVISA Registration Number: 80844240002
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Related Devices (2)

Teste Rápido Pantest Coronavirus IgM/IgG
Risk Class III

Registration Details

80844240002

25351735674202021

14112327000160

Company Information

PANTEST SA
Portugal
PT: PORTUGAL

Dates and Status

Dec 07, 2020

07/12/2030

09/18/2025 19:00:01

Teste Rápido Pantest Coronavirus IgM/IgG
Risk Class III

Registration Details

80844240002

25351735674202021

14112327000160

Company Information

Dates and Status

Dec 07, 2020

07/12/2030

09/18/2025 19:00:01