ANVISA registration

Família EliA ANCA/GBM Control

Registration 80254180306. PARÂMETROS COMBINADOS NO MESMO PRODUTO - CLASSE II

Registration details

Registration number80254180306
Application number25351610988201717
Technical namePARÂMETROS COMBINADOS NO MESMO PRODUTO - CLASSE II
Risk classII
Published on16/07/2018
ValidityIndefinite validity

Registration holder

Legal namePHADIA DIAGNOSTICOS LTDA
CNPJ04.930.429/0001-39

Manufacturer

  • PHADIA AB SUÉCIA

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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