Instrument for sample preparation and processing – pre-analytical phase - ANVISA Registration 80223480092
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 80223480092 and manufactured by DLAB SCIENTIFIC CO., LTD. The registration is held by MH EQUIPAMENTOS E MATERIAIS PARA LABORATORIOS LTDA EPP with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 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.
Device Details
Registration Details
80223480092
25351297534202211
04342755000125
Company Information
Dates and Status
Sep 22, 2022
VIGENTE
09/18/2025 19:00:01
EPPENDORF SE• Germany
SHANDON DIAGNOSTICS LIMITED• United Kingdom
BECKMAN COULTER, INC.• United States of America
JIANGSU KANGJIAN MEDICAL APPARATUS CO. LTD.• China
CHANGZHOU HAOSILIN MEDICAL INSTRUMENT CO.,LTD• China
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