Instrument for sample preparation and processing – pre-analytical phase - ANVISA Registration 81585500015

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 81585500015 and manufactured by ZHEJIANG JINHUA KEDI INSTRUMENTAL EQUIPAMENT CO., LTD. The registration is held by LUPE INDUSTRIA TECNOLOGICA DE EQUIPAMENTOS PARA LABORATORIO 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.