ANVISA registration 80367750039Active

LYSIS SOLUTION

Name: LYSIS SOLUTION — ANVISA registration 80367750039
Creator: NORMA INSTRUMENTS ZRT.
Keywords: LYSIS SOLUTION, SOLUÇÃO DE LISE, Solução de Lise 5 Diff, 80367750039, Risk Class I, ANVISA registration

ANVISA Registration Number: 80367750039BIOSYSTEMS NE COMÉRCIO DE PRODUTOS LABORATORIAIS E HOSPITALARES LTDANORMA INSTRUMENTS ZRT.Risk Class I

Verified

Device names

Technical name: LYSIS SOLUTION
Commercial name: Solução de Lise 5 Diff
Risk class: Class I

Registration details

Registration Number: 80367750039
Process Number: 25351791927201822
CNPJ: 08282077000103

Company information

Registration Holder: BIOSYSTEMS NE COMÉRCIO DE PRODUTOS LABORATORIAIS E HOSPITALARES LTDA
Manufacturer: NORMA INSTRUMENTS ZRT.
Manufacturing Country: Hungary

Dates and status

Publication Date: Feb 11, 2019
Validity: VIGENTE
Last Updated: 08/18/2026 19:00:00

About this record

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 80367750039 and manufactured by NORMA INSTRUMENTS ZRT.. The registration is held by BIOSYSTEMS NE COMÉRCIO DE PRODUTOS LABORATORIAIS E HOSPITALARES LTDA with validity until currently active (VIGENTE).

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