TOXOPLASMA GONDII - ANVISA Registration 10338930114

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 10338930114 and manufactured by EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG. The registration is held by EUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDA with validity until Aug 25, 2034.

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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10338930114
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Registration Details
ANVISA Registration Number: 10338930114
Janaina dos Santos de Miranda

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Related Devices (2)

Toxoplasma gondii (IgM)
Risk Class IV

Registration Details

10338930114

25351291791201401

93741726000166

Company Information

Germany
PT: ALEMANHA

Dates and Status

Aug 25, 2014

25/08/2034

09/18/2025 19:00:01

Toxoplasma gondii (IgM)
Risk Class IV

Registration Details

10338930114

25351291791201401

93741726000166

Company Information

Dates and Status

Aug 25, 2014

25/08/2034

09/18/2025 19:00:01