TOXOPLASMA GONDII - ANVISA Registration 10345160726

Access comprehensive regulatory information for TOXOPLASMA GONDII in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 10345160726 and manufactured by manufacturer not specified. The registration is held by SIEMENS HEALTHCARE DIAGNÓSTICOS LTDA with validity until Jun 30, 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 ABBOTT GMBH, ROCHE DIAGNOSTICS GMBH, 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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10345160726
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Registration Details
ANVISA Registration Number: 10345160726
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Related Devices (2)

TOXOPLASMA IgG QUANTITATIVO IMMULITE / IMMULITE 1000
Risk Class IV

Registration Details

10345160726

25351038498200890

01449930000190

Company Information

Dates and Status

Jun 30, 2008

30/06/2033

09/18/2025 19:00:01

TOXOPLASMA IgG QUANTITATIVO IMMULITE / IMMULITE 1000
Risk Class IV

Registration Details

10345160726

25351038498200890

01449930000190

Company Information

United Kingdom
PT: REINO UNIDO

Dates and Status

Jun 30, 2008

30/06/2033

09/18/2025 19:00:01