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DENGUE - ANVISA Registration 80859840229

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 80859840229 and manufactured by manufacturer not specified. The registration is held by CPMH - Comércio e Indústria de Produtos Médico-Hospitalares e Odontológicos LTDA. with validity until Apr 22, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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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80859840229
2 Related Devices
Registration Details
ANVISA Registration Number: 80859840229
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Related Devices (2)

Dengue Combo Rapid Test
Risk Class III

Registration Details

80859840229

25351295548202454

13532259000125

Dates and Status

Apr 22, 2025

22/04/2035

09/18/2025 19:00:01

Dengue Combo Rapid Test
Risk Class III

Registration Details

80859840229

25351295548202454

13532259000125

Company Information

Dates and Status

Apr 22, 2025

22/04/2035

09/18/2025 19:00:01