ANVISA registration

EliA GBM Well

Registration 80254180386. ANTICORPO ANTIMEMBRANA BASAL GLOMERULAR (GMB)

Registration details

Registration number80254180386
Application number25351363128202165
Technical nameANTICORPO ANTIMEMBRANA BASAL GLOMERULAR (GMB)
Risk classII
Published on06/05/2021
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.

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