LYSIS SOLUTION - ANVISA Registration 80146502398

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 80146502398 and manufactured by ABBOTT IRELAND DIAGNOSTICS DIVISION. The registration is held by ABBOTT LABORATORIOS DO BRASIL 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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80146502398
Registration Details
ANVISA Registration Number: 80146502398
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

Folate Lysis Reagent
Risk Class I

Registration Details

80146502398

25351019675202530

56998701000116

Company Information

Ireland
PT: IRLANDA

Dates and Status

Mar 05, 2025

VIGENTE

09/18/2025 19:00:01