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LYSIS SOLUTION - ANVISA Registration 80019640096

Access comprehensive regulatory information for LYSIS SOLUTION in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80019640096 and manufactured by DIAGNO SOLUÇÕES EM DIAGNÓSTICO LTDA. The registration is held by DIAGNO SOLUÇÕES EM DIAGNÓSTICO 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 DIAGNO SOLUÇÕES EM DIAGNÓSTICO LTDA, 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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80019640096
Registration Details
ANVISA Registration Number: 80019640096
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Device Details

Cellalyse Diff I
Risk Class I

Registration Details

80019640096

25351019639202576

01866908000145

Company Information

Brazil
PT: BRASIL

Dates and Status

Mar 05, 2025

VIGENTE

09/18/2025 19:00:01