LYSIS SOLUTION - ANVISA Registration 80015490008

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 80015490008 and manufactured by SYSMEX CORPORATION. The registration is held by SYSMEX DO BRASIL INDUSTRIA E COMERCIO LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for 3 related devices, 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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80015490008
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Registration Details
ANVISA Registration Number: 80015490008
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (3)

STROMATOLYSER WH
Risk Class I

Registration Details

80015490008

253510189800011

02923414000118

Company Information

SYSMEX CORPORATION
Japan
PT: JAPÃO

Dates and Status

Oct 09, 2000

VIGENTE

09/18/2025 19:00:01

STROMATOLYSER WH
Risk Class I

Registration Details

80015490008

253510189800011

02923414000118

Company Information

Brazil
PT: BRASIL

Dates and Status

Oct 09, 2000

VIGENTE

09/18/2025 19:00:01

STROMATOLYSER WH
Risk Class I

Registration Details

80015490008

253510189800011

02923414000118

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Oct 09, 2000

VIGENTE

09/18/2025 19:00:01