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Instrument for cell and platelet analysis or counting - ANVISA Registration 81154840007

Access comprehensive regulatory information for Instrument for cell and platelet analysis or counting in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81154840007 and manufactured by B&E DIAGNOSTICS INC.. The registration is held by Biomedtech do Brasil Produtos Médicos e Diagnósticos 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 SHENZHEN DYMIND BIOTECHNOLOGY CO., LTD, SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD, 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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81154840007
Registration Details
ANVISA Registration Number: 81154840007
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Device Details

Família de Analisadores Automáticos de Hematologia Hemax Série 300
Risk Class II

Registration Details

81154840007

25351161574201703

13016094000139

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jun 05, 2017

VIGENTE

09/18/2025 19:00:01