ZIKA - ANVISA Registration 80345000256

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 80345000256 and manufactured by DIA PRO DIAGNOSTIC BIOPROBES S.R.L.. The registration is held by GOYAZES BIOTECNOLOGIA LTDA with validity until Jul 30, 2028.

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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80345000256
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Registration Details
ANVISA Registration Number: 80345000256
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Zika IgG Test
Risk Class IV

Registration Details

80345000256

25351197098201897

05658906000111

Company Information

Italy
PT: ITÁLIA

Dates and Status

Jul 30, 2018

30/07/2028

09/18/2025 19:00:01

Zika IgG Test
Risk Class IV

Registration Details

80345000256

25351197098201897

05658906000111

Company Information

Dates and Status

Jul 30, 2018

30/07/2028

09/18/2025 19:00:01