TOXOPLASMA GONDII - ANVISA Registration 10345161025

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 10345161025 and manufactured by MISONIX, INC. The registration is held by SIEMENS HEALTHCARE DIAGNÓSTICOS LTDA with validity until Dec 22, 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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10345161025
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Registration Details
ANVISA Registration Number: 10345161025
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Toxoplasma Quantitativo IgG IMMULITE 2000
Risk Class IV

Registration Details

10345161025

25351026573200870

01449930000190

Company Information

MISONIX, INC
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Dec 22, 2008

22/12/2033

09/18/2025 19:00:01

Toxoplasma Quantitativo IgG IMMULITE 2000
Risk Class IV

Registration Details

10345161025

25351026573200870

01449930000190

Company Information

Dates and Status

Dec 22, 2008

22/12/2033

09/18/2025 19:00:01