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CHIKUNGUNYA - ANVISA Registration 81268670001

Access comprehensive regulatory information for CHIKUNGUNYA in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81268670001 and manufactured by LUMIQUICK DIAGNOSTICS, INC. The registration is held by ONEWAY IMPORTADORA E DISTRIBUIDORA LTDA with validity until Jan 30, 2027.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including Eco Diagnostica Ltda, VIRCELL MICROBIOLOGISTS, 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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81268670001
2 Related Devices
Registration Details
ANVISA Registration Number: 81268670001
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Related Devices (2)

QuickProfile® Chikungunya IgG/IgM Combo Test Card
Risk Class III

Registration Details

81268670001

25351280776201635

13605812000102

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jan 30, 2017

30/01/2027

09/18/2025 19:00:01

QuickProfile® Chikungunya IgG/IgM Combo Test Card
Risk Class III

Registration Details

81268670001

25351280776201635

13605812000102

Company Information

Dates and Status

Jan 30, 2017

30/01/2027

09/18/2025 19:00:01