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ANVISA registration 80003610580Active

AUTOIMMUNE HEPATITIS (AIH) ANTIBODY

ANVISA Registration Number: 80003610580WERFEN MEDICAL LTDAINOVA DIAGNOSTICS, INC.Risk Class II
Verified
Device names
Technical name
AUTOIMMUNE HEPATITIS (AIH) ANTIBODY
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PT: ANTICORPO PARA HEPATITE AUTOIMUNE (HAI)
Commercial name
Família QUANTA Flash LKM-1
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Risk class
Class II
Registration details
Registration Number
80003610580
Process Number
25351286519202078
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 10, 2020
Status
Active
Official value: VIGENTE
About this record

Access comprehensive regulatory information for AUTOIMMUNE HEPATITIS (AIH) ANTIBODY in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80003610580 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.