ANVISA registration

Teste de Gravidez (hCG) - Midstream 10mUI/mL

Registration 82832860022. AUTOTESTE PARA GONADOTROFINA CORIÔNICA HUMANA (HCG)

Registration details

Registration number82832860022
Application number25351393031202420
Technical nameAUTOTESTE PARA GONADOTROFINA CORIÔNICA HUMANA (HCG)
Risk classII
Published on23/09/2024
ValidityIndefinite validity

Registration holder

Legal nameQLX DIAGNÓSTICOS LTDA
CNPJ38.030.634/0001-60

Manufacturer

  • HANGZHOU LAIHE BIOTECH CO., LTD. CHINA, REPÚBLICA POPULAR

Other registrations held by QLX DIAGNÓSTICOS LTDAview all

LISANTE H HMG86

82832860002

DETERGENTE CD800

82832860003

LISANTE D HMG86

82832860005

LISANTE 3D

82832860008

DILUENTE HMG86

82832860009

DILUENTE 3D

82832860010

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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