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ANVISA registration 80231270012Active

Instrumento para preparo e processamento de amostras – fase pré-analítica

ANVISA Registration Number: 80231270012QUIMIS APARELHOS CIENTIFICOS LIMITADAQUIMIS APARELHOS CIENTIFICOS LIMITADARisk Class I
Device names
Technical name
Instrumento para preparo e processamento de amostras – fase pré-analítica
Commercial name
CENTRÍFUGA DIGITAL MULTIANÁLISES
Risk class
Class I
Registration details
Registration Number
80231270012
Process Number
25351073087202541
CNPJ
48071377000168
Company information
Manufacturing Country
Brazil
PT: BRASIL
Dates and status
Publication Date
Jun 09, 2025
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Instrumento para preparo e processamento de amostras – fase pré-analítica in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80231270012 and manufactured by QUIMIS APARELHOS CIENTIFICOS LIMITADA. The registration is held by QUIMIS APARELHOS CIENTIFICOS LIMITADA with validity until currently active (VIGENTE).

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