IMMUNOGLOBULIN E - ANVISA Registration 80254180035
Access comprehensive regulatory information for IMMUNOGLOBULIN E in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80254180035 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, 5 companies making the same product including PHADIA AB, SHENZHEN DYMIND BIOTECHNOLOGY CO., LTD, 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.

Janaina dos Santos de Miranda
š§š· Brazil Regulatory Expert
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Registration Details
80254180035
25351280451200584
04930429000139
Company Information
Dates and Status
Oct 17, 2005
VIGENTE
09/18/2025 19:00:01
IMMUNOGLOBULIN E
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AESKUCAREĀ® Allergy ONE
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AESKUCAREĀ® Allergy TWO
AESKU DIAGNOSTICS GMBH & CO. KG
80105220274
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IMUNOGLOBULINA E
AESKUCAREĀ® Allergy FOUR
AESKU DIAGNOSTICS GMBH & CO. KG
80105220275
Jun 16, 2025
IMUNOGLOBULINA E
AESKUCAREĀ® Allergy THREE
AESKU DIAGNOSTICS GMBH & CO. KG
80105220276
Jun 16, 2025