LYSIS SOLUTION - ANVISA Registration 81996070038

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 81996070038 and manufactured by DIAGFAST PRODUTOS PARA LABORATORIOS LTDA. The registration is held by DIAGFAST PRODUTOS PARA LABORATORIOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 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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81996070038
Registration Details
ANVISA Registration Number: 81996070038
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

LISE DIAG DXH
Risk Class I

Registration Details

81996070038

25351685502202181

30984754000194

Company Information

Brazil
PT: BRASIL

Dates and Status

Nov 11, 2021

VIGENTE

09/18/2025 19:00:01