TREPONEMA PALLIDUM - ANVISA Registration 10071770820

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 10071770820 and manufactured by ABON BIOPHARM (HANGZHOU) CO LTD. The registration is held by ABBOTT DIAGNOSTICOS RAPIDOS S.A. with validity until Dec 26, 2026.

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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10071770820
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Registration Details
ANVISA Registration Number: 10071770820
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Syphilis Ultra Rapid Test
Risk Class IV

Registration Details

10071770820

25351003940201582

50248780000161

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Mar 30, 2015

26/12/2026

09/18/2025 19:00:01

Syphilis Ultra Rapid Test
Risk Class IV

Registration Details

10071770820

25351003940201582

50248780000161

Company Information

Dates and Status

Mar 30, 2015

26/12/2026

09/18/2025 19:00:01