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ANVISA registration 80788620036Active

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

ANVISA Registration Number: 80788620036NIPRO MEDICAL CORPORATION PRODUTOS MÉDICOS LTDADRUCKER DIAGNOSTICSRisk Class I
Device names
Technical name
Instrumento para preparo e processamento de amostras – fase pré-analítica
Commercial name
FAMÍLIA DE CENTRÍFUGAS DRUCKER
Risk class
Class I
Registration details
Registration Number
80788620036
Process Number
25351482042201607
CNPJ
13333090000184
Company information
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Mar 27, 2017
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 80788620036 and manufactured by DRUCKER DIAGNOSTICS. The registration is held by NIPRO MEDICAL CORPORATION PRODUTOS MÉDICOS LTDA with validity until currently active (VIGENTE).

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