LYSIS SOLUTION - ANVISA Registration 81327670016

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 81327670016 and manufactured by DIATRON MI ZRT.. The registration is held by DNEDX COMERCIO E SERVICOS PARA PRODUTOS DA SAUDE 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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81327670016
Registration Details
ANVISA Registration Number: 81327670016
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

LUMIRATEK LYSE-5P
Risk Class I

Registration Details

81327670016

25351187381201608

22940751000120

Company Information

DIATRON MI ZRT.
Hungary
PT: HUNGRIA

Dates and Status

Sep 05, 2016

VIGENTE

09/18/2025 19:00:01