LYSIS SOLUTION - ANVISA Registration 10303460163

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 10303460163 and manufactured by manufacturer not specified. 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 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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10303460163
Registration Details
ANVISA Registration Number: 10303460163
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

HC-LYSE CF
Risk Class I

Registration Details

10303460163

25351327342200919

42837716000198

Company Information

Dates and Status

May 31, 2010

VIGENTE

09/18/2025 19:00:01