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REAGENT / SYSTEM FOR PLATELET AGGREGATION - ANVISA Registration 10230730190

Access comprehensive regulatory information for REAGENT / SYSTEM FOR PLATELET AGGREGATION in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10230730190 and manufactured by HELENA LABORATORIES INC.. The registration is held by NL COMÉRCIO EXTERIOR 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 HELENA LABORATORIES, 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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10230730190
Registration Details
ANVISA Registration Number: 10230730190
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Device Details

Registration Details

10230730190

25351461008202394

52541273000147

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Aug 28, 2023

VIGENTE

09/18/2025 19:00:01