DENGUE - ANVISA Registration 10071770730

Access comprehensive regulatory information for DENGUE in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10071770730 and manufactured by manufacturer not specified. The registration is held by ABBOTT DIAGNOSTICOS RAPIDOS S.A. with validity until Oct 27, 2033.

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, HANGZHOU ALLTEST BIOTECH CO. LTD, 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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10071770730
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Registration Details
ANVISA Registration Number: 10071770730
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

BIOLINE Dengue Duo
Risk Class III

Registration Details

10071770730

25351135424201333

50248780000161

Company Information

Dates and Status

Jun 03, 2013

27/10/2033

09/18/2025 19:00:01

BIOLINE Dengue Duo
Risk Class III

Registration Details

10071770730

25351135424201333

50248780000161

Company Information

South Korea
PT: CORÉIA DO SUL

Dates and Status

Jun 03, 2013

27/10/2033

09/18/2025 19:00:01