ANVISA registration

CEDIA® Core TDM Multi-Calibrators

Registration 80254180381. PARÂMETROS COMBINADOS NO MESMO PRODUTO - CLASSE III

Registration details

Registration number80254180381
Application number25351644040202061
Technical namePARÂMETROS COMBINADOS NO MESMO PRODUTO - CLASSE III
Risk classIII
Published on30/12/2020
ValidityValid until 30/12/2030

Registration holder

Legal namePHADIA DIAGNOSTICOS LTDA
CNPJ04.930.429/0001-39

Manufacturer

  • MICROGENICS CORPORATION ESTADOS UNIDOS DA AMÉRICA

Other registrations held by PHADIA DIAGNOSTICOS LTDAview all

PHADIATOP IMMUNOCAP

80254180002

STOP SOLUTION

80254180003

IMMUNOCAP IGA/IGG CALIBRATOR IMMUNOCAP

80254180004

DEVELOPMENT SOLUTION

80254180005

Família ImmunoCAP Allergen Sementes e Cereais

80254180007

WASHING SOLUTION

80254180008

Source: ANVISA

Source: ANVISA open data, medical device file, updated daily. The public database provides registration validity, rather than registration status: this registration may have been cancelled before its expiry date without this being shown here. Before making purchasing, import or marketing decisions, check the ANVISA search portal.

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