IMMUNOGLOBULIN E - ANVISA Registration 80464810432
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 80464810432 and manufactured by VEDALAB. The registration is held by ARGOSLAB DISTRIBUIDORA DE PRODUTOS PARA LABORATÓRIOS 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.

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Registration Details
80464810432
25351085166201539
09377976000152
Company Information
Dates and Status
Apr 13, 2015
VIGENTE
09/18/2025 19:00:01
IMMUNOGLOBULIN E
IgE-CHECK-1 Qualitative
VEDALAB
80464810841
Aug 14, 2023
IMMUNOGLOBULIN E
ALLERGY-Check®
VEDALAB
80464810657
May 06, 2019
IMMUNOGLOBULIN E
IgE
RADIM SPA
80103990063
Feb 05, 2007
IMMUNOGLOBULIN E
IgE
VYTTRA DIAGNOSTICOS S.A.
81692610201
Oct 01, 2020
IMMUNOGLOBULIN E
IgE
KATAL BIOTECNOLOGICA INDÚSTRIA E COMÉRCIO LTDA
10377390220
Dec 28, 2015
IMUNOGLOBULINA E
Celer Finecare IgE Teste Quantitativo
GUANGZHOU WONDFO BIOTECH CO. LTD
80537410147
Jul 14, 2025
IMUNOGLOBULINA E
AESKUCARE® Allergy ONE
AESKU DIAGNOSTICS GMBH & CO. KG
80105220273
Jun 16, 2025
IMUNOGLOBULINA E
AESKUCARE® Allergy TWO
AESKU DIAGNOSTICS GMBH & CO. KG
80105220274
Jun 16, 2025
IMUNOGLOBULINA E
AESKUCARE® Allergy FOUR
AESKU DIAGNOSTICS GMBH & CO. KG
80105220275
Jun 16, 2025
IMUNOGLOBULINA E
AESKUCARE® Allergy THREE
AESKU DIAGNOSTICS GMBH & CO. KG
80105220276
Jun 16, 2025