TREPONEMA PALLIDUM - ANVISA Registration 80524900052

Access comprehensive regulatory information for TREPONEMA PALLIDUM in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80524900052 and manufactured by manufacturer not specified. The registration is held by BIO ADVANCE DIAGNOSTICOS LTDA with validity until Feb 06, 2027.

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 WAMA PRODUTOS PARA LABORATORIO LTDA, EUROIMMUN AG, 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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80524900052
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Registration Details
ANVISA Registration Number: 80524900052
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

TESTE RÁPIDO ONSITE SÍFILIS Ab COMBO
Risk Class IV

Registration Details

80524900052

25351228161201689

09593438000103

Company Information

Dates and Status

Feb 06, 2017

06/02/2027

09/18/2025 19:00:01

TESTE RÁPIDO ONSITE SÍFILIS Ab COMBO
Risk Class IV

Registration Details

80524900052

25351228161201689

09593438000103

Company Information

CTK BIOTECH, INC.
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Feb 06, 2017

06/02/2027

09/18/2025 19:00:01