ZIKA - ANVISA Registration 10330660254

Access comprehensive regulatory information for ZIKA in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 10330660254 and manufactured by SD BIOSENSOR, INC.. The registration is held by DESCARPACK DESCARTAVEIS DO BRASIL LTDA with validity until Jul 01, 2029.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including Eco Diagnostica Ltda, VIRCELL S.L., 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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10330660254
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Registration Details
ANVISA Registration Number: 10330660254
Janaina dos Santos de Miranda

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Related Devices (2)

Teste Rápido Standard Q Zika IgM
Risk Class IV

Registration Details

10330660254

25351797820201898

01057428000133

Company Information

SD BIOSENSOR, INC.
South Korea
PT: CORÉIA DO SUL

Dates and Status

Jul 01, 2019

01/07/2029

09/18/2025 19:00:01

Teste Rápido Standard Q Zika IgM
Risk Class IV

Registration Details

10330660254

25351797820201898

01057428000133

Company Information

Dates and Status

Jul 01, 2019

01/07/2029

09/18/2025 19:00:01