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ANVISA registration 80254180417Active

IMMUNOGLOBULIN G SUBCLASS (IgG1/IgG2/IgG3/IgG4)

ANVISA Registration Number: 80254180417PHADIA DIAGNOSTICOS LTDAPHADIA ABRisk Class II
Verified
Device names
Technical name
IMMUNOGLOBULIN G SUBCLASS (IgG1/IgG2/IgG3/IgG4)
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PT: SUBCLASSE DE IMUNOGLOBULINA G (IgG1/IgG2/IgG3/IgG4)
Commercial name
Família ImmunoCAP Specific IgG4
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Risk class
Class II
Registration details
Registration Number
80254180417
Process Number
25351500131202257
CNPJ
04930429000139
Company information
Registration Holder
PHADIA DIAGNOSTICOS LTDA
Manufacturer
PHADIA AB
Manufacturing Country
Sweden
PT: SUÉCIA
Dates and status
Publication Date
May 19, 2022
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for IMMUNOGLOBULIN G SUBCLASS (IgG1/IgG2/IgG3/IgG4) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80254180417 and manufactured by PHADIA AB. The registration is held by PHADIA DIAGNOSTICOS LTDA with validity until currently active (VIGENTE).

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.