LYSIS SOLUTION - ANVISA Registration 10347320008

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 10347320008 and manufactured by HORIBA ABX. The registration is held by HORIBA INSTRUMENTS BRASIL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for 2 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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10347320008
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Registration Details
ANVISA Registration Number: 10347320008
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

ABX MINILYSE LMG
Risk Class I

Registration Details

10347320008

250000215019856

01759236000179

Company Information

HORIBA ABX
France
PT: FRANÇA

Dates and Status

Sep 24, 1998

VIGENTE

09/18/2025 19:00:01

ABX MINILYSE LMG
Risk Class I

Registration Details

10347320008

250000215019856

01759236000179

Company Information

Brazil
PT: BRASIL

Dates and Status

Sep 24, 1998

VIGENTE

09/18/2025 19:00:01