IMMUNOGLOBULIN E - ANVISA Registration 80524900008
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 80524900008 and manufactured by PISHTAZ TEB ZAMAN DIAGNOSTICS CO. The registration is held by BIO ADVANCE DIAGNOSTICOS LTDA 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 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.
Device Details
Registration Details
80524900008
25351594830200989
09593438000103
Company Information
Dates and Status
Mar 08, 2010
VIGENTE
09/18/2025 19:00:01
IMUNOGLOBULINA E
Celer Finecare IgE Teste Quantitativo
GUANGZHOU WONDFO BIOTECH CO. LTD
80537410147
Jul 14, 2025
IMUNOGLOBULINA E
AESKUCAREยฎ Allergy ONE
AESKU DIAGNOSTICS GMBH & CO. KG
80105220273
Jun 16, 2025
IMUNOGLOBULINA E
AESKUCAREยฎ Allergy TWO
AESKU DIAGNOSTICS GMBH & CO. KG
80105220274
Jun 16, 2025
IMUNOGLOBULINA E
AESKUCAREยฎ Allergy FOUR
AESKU DIAGNOSTICS GMBH & CO. KG
80105220275
Jun 16, 2025
IMUNOGLOBULINA E
AESKUCAREยฎ Allergy THREE
AESKU DIAGNOSTICS GMBH & CO. KG
80105220276
Jun 16, 2025

