EOSINOPHIL CATIONIC PROTEIN - ANVISA Registration 80254180320
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 80254180320 and manufactured by PHADIA AB. The registration is held by PHADIA DIAGNOSTICOS 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, 2 companies making the same product including SIEMENS HEALTHCARE DIAGNOSTICS INC., 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.

Janaina dos Santos de Miranda
🇧🇷 Brazil Regulatory Expert
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Registration Details
80254180320
25351306355201979
04930429000139
Company Information
Dates and Status
Sep 09, 2019
VIGENTE
09/18/2025 19:00:01
IMMUNOGLOBULIN E
IMMUNOCAP SPECIFIC IGE ANTI-IGE
PHADIA AB
80254180020
Sep 19, 2005
IMMUNOGLOBULIN E
ImmunoCAP ISAC E112i
PHADIA AB
80254180338
Jan 13, 2020
IMMUNOGLOBULIN E
IMMUNOCAP TOTAL IGE ANTI-IGE
PHADIA AB
80254180015
Sep 12, 2005
IMMUNOGLOBULIN E
IMMUNOCAP SPECIFIC IGE CONJUGATE 400
PHADIA AB
80254180012
Sep 12, 2005
IMMUNOGLOBULIN E
ImmunoCAP Total IgE Conjugate 400
PHADIA AB
80254180109
Mar 23, 2009
PROTEÍNA CATIÔNICA EOSINÓFILA
IMMULITE 2000 ECP
SIEMENS HEALTHCARE DIAGNOSTICS INC.
10345161851
May 14, 2012
PROTEÍNA CATIÔNICA EOSINÓFILA
IMMULITE / IMMULITE 1000 ECP
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED
10345161774
Nov 03, 2010