ANVISA registration

Família MAS Liquimmune

Registration 80254180362. PARÂMETROS COMBINADOS NO MESMO PRODUTO - CLASSE III

Registration details

Registration number80254180362
Application number25351080623202051
Technical namePARÂMETROS COMBINADOS NO MESMO PRODUTO - CLASSE III
Risk classIII
Published on27/07/2020
ValidityValid until 27/07/2030

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.

Next step

Medical device registration with ANVISA

HSC manages the process from risk classification to liaising with the regulator, in Brazil and more than 40 other countries.

Speak to a specialist