TREPONEMA PALLIDUM - ANVISA Registration 81148560046

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 81148560046 and manufactured by manufacturer not specified. The registration is held by EUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDA with validity until Mar 27, 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 MEDIZINISCHE LABORDIAGNOSTIKA 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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81148560046
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Registration Details
ANVISA Registration Number: 81148560046
Janaina dos Santos de Miranda

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Related Devices (2)

Treponema pallidum Screen
Risk Class IV

Registration Details

81148560046

25351410774201619

93741726000166

Company Information

Dates and Status

Mar 27, 2017

27/03/2027

09/18/2025 19:00:01

Treponema pallidum Screen
Risk Class IV

Registration Details

81148560046

25351410774201619

93741726000166

Company Information

EUROIMMUN AG
Germany
PT: ALEMANHA

Dates and Status

Mar 27, 2017

27/03/2027

09/18/2025 19:00:01