Instrument for sample preparation and processing – pre-analytical phase - ANVISA Registration 80019789013
Access comprehensive regulatory information for Instrument for sample preparation and processing – pre-analytical phase in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80019789013 and manufactured by EPPENDORF SE. The registration is held by EPPENDORF DO BRASIL LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including EPPENDORF SE, SHANDON DIAGNOSTICS LIMITED, 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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Registration Details
80019789013
25351459470200540
03010937000136
Company Information
Dates and Status
Mar 20, 2006
VIGENTE
09/18/2025 19:00:01
Instrument for sample preparation and processing – pre-analytical phase
CENTRIFUGA NÃO REFRIGERADA
EPPENDORF SE
80019789008
Mar 08, 2004
Instrument for sample preparation and processing – pre-analytical phase
CENTRIFUGA NAO REFRIGERADA 5810
EPPENDORF SE
80019789012
Mar 20, 2006
Instrument for sample preparation and processing – pre-analytical phase
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80241710023
Apr 10, 2017
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Nov 21, 2022
Instrument for sample preparation and processing – pre-analytical phase
CENTRIFUGA
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80019789005
Feb 03, 2004
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Instrumento para preparo e processamento de amostras – fase pré-analítica
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