EOSINOPHIL CATIONIC PROTEIN - ANVISA Registration 10345161851
Access comprehensive regulatory information for EOSINOPHIL CATIONIC PROTEIN in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10345161851 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.. The registration is held by SIEMENS HEALTHCARE DIAGNÓSTICOS LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 2 companies making the same product including PHADIA AB, SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED, and 2 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
10345161851
25351116524201203
01449930000190
Company Information
Dates and Status
May 14, 2012
VIGENTE
09/18/2025 19:00:01
PROTEÍNA CATIÔNICA EOSINÓFILA
ImmunoCAP ECP anti-ECP
PHADIA AB
80254180320
Sep 09, 2019
PROTEÍNA CATIÔNICA EOSINÓFILA
IMMULITE / IMMULITE 1000 ECP
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED
10345161774
Nov 03, 2010

