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ANVISA registration 81826160090Active

FERRITIN

ANVISA Registration Number: 81826160090ERBA DIAGNOSTICS BRAZIL, PRODUCAO E DISTRIBUICAO DE PRODUTOS MEDICOS LTDAERBA LACHEMA S.R.O.Risk Class II
Device names
Technical name
FERRITIN
PT: FERRITINA
Risk class
Class II
Registration details
Registration Number
81826160090
Process Number
25351519595202237
CNPJ
32190515000198
Company information
Manufacturing Country
Czechia
PT: TCHECA, REPÚBLICA
Dates and status
Publication Date
May 26, 2022
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for FERRITIN in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81826160090 and manufactured by ERBA LACHEMA S.R.O.. The registration is held by ERBA DIAGNOSTICS BRAZIL, PRODUCAO E DISTRIBUICAO DE PRODUTOS MEDICOS LTDA with validity until currently active (VIGENTE).

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