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ANVISA registration 10337990011Active

EQUIPMENT FOR PREPARING SAMPLES FOR IN VITRO DIAGNOSTICS

ANVISA Registration Number: 10337990011LEICA DO BRASIL IMPORTAÇÃO E COMÉRCIO LTDA.Leica Biosystems Nussloch GmbHRisk Class I
Device names
Technical name
EQUIPMENT FOR PREPARING SAMPLES FOR IN VITRO DIAGNOSTICS
PT: EQUIPAMENTO PARA PREPARO DE AMOSTRAS PARA DIAGNÓSTICO IN VITRO
Commercial name
Corador de Tecidos
Risk class
Class I
Registration details
Registration Number
10337990011
Process Number
25351560681201513
CNPJ
52201456000113
Company information
Manufacturing Country
Germany
PT: ALEMANHA
Dates and status
Publication Date
Nov 03, 2015
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for EQUIPMENT FOR PREPARING SAMPLES FOR IN VITRO DIAGNOSTICS in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10337990011 and manufactured by Leica Biosystems Nussloch GmbH. The registration is held by LEICA DO BRASIL IMPORTAÇÃO E COMÉRCIO LTDA. with validity until currently active (VIGENTE).

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