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CORONAVIRUS - ANVISA Registration 80102512697

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 80102512697 and manufactured by manufacturer not specified. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Sep 06, 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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80102512697
2 Related Devices
Registration Details
ANVISA Registration Number: 80102512697
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Related Devices (2)

Família Teste RAMP® Antígeno COVID-19
Risk Class III

Registration Details

80102512697

25351764827202129

04718143000194

Dates and Status

Sep 06, 2021

06/09/2031

09/18/2025 19:00:01

Família Teste RAMP® Antígeno COVID-19
Risk Class III

Registration Details

80102512697

25351764827202129

04718143000194

Company Information

Canada
PT: CANADÁ

Dates and Status

Sep 06, 2021

06/09/2031

09/18/2025 19:00:01