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Instrument for cell and platelet analysis or counting - ANVISA Registration 10303460564

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 10303460564 and manufactured by IN VITRO DIAGNOSTICA LTDA. The registration is held by IN VITRO DIAGNOSTICA 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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10303460564
Registration Details
ANVISA Registration Number: 10303460564
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Device Details

Família de Analisadores Semi-Automáticos de Hematologia Blood 3P
Risk Class II

Registration Details

10303460564

25351128274202570

42837716000198

Company Information

Brazil
PT: BRASIL

Dates and Status

Sep 08, 2025

VIGENTE

09/18/2025 19:00:01