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ANVISA registration 80003610582Active

ANTI-GLOMERULAR BASEMENT MEMBRANE ANTIBODY (GBM)

ANVISA Registration Number: 80003610582WERFEN MEDICAL LTDAINOVA DIAGNOSTICS, INC.Risk Class II
Verified
Device names
Technical name
ANTI-GLOMERULAR BASEMENT MEMBRANE ANTIBODY (GBM)
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PT: ANTICORPO ANTIMEMBRANA BASAL GLOMERULAR (GMB)
Commercial name
Família QUANTA Flash GBM
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Risk class
Class II
Registration details
Registration Number
80003610582
Process Number
25351477045202071
CNPJ
02004662000165
Company information
Registration Holder
WERFEN MEDICAL LTDA
Manufacturer
INOVA DIAGNOSTICS, INC.
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Aug 31, 2020
Status
Active
Official value: VIGENTE
About this record

Access comprehensive regulatory information for ANTI-GLOMERULAR BASEMENT MEMBRANE ANTIBODY (GBM) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80003610582 and manufactured by INOVA DIAGNOSTICS, INC.. The registration is held by WERFEN MEDICAL 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.