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FOLATE - ANVISA Registration 80836930125

Access comprehensive regulatory information for FOLATE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80836930125 and manufactured by IMMUNDIAGNOSTIK AG. The registration is held by ARBO DISTRIBUIDORA DE PRODUTOS PARA LABORATÓRIOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including ROCHE DIAGNOSTICS GMBH, ABBOTT IRELAND DIAGNOSTICS DIVISION, 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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80836930125
Registration Details
ANVISA Registration Number: 80836930125
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Device Details

ID-Vit® Folic acid in whole blood
Risk Class II

Registration Details

80836930125

25351419810202462

06203702000159

Company Information

IMMUNDIAGNOSTIK AG
Germany
PT: ALEMANHA

Dates and Status

Jan 06, 2025

VIGENTE

09/18/2025 19:00:01