ANVISA registration

Teste Rápido Standard Q Febre Amarela IgM

Registration 10330660287. FEBRE AMARELA

Registration details

Registration number10330660287
Application number25351696314201963
Technical nameFEBRE AMARELA
Risk classIII
Published on02/03/2020
ValidityValid until 02/03/2030

Registration holder

Legal nameDESCARPACK DESCARTAVEIS DO BRASIL LTDA
CNPJ01.057.428/0001-33

Manufacturer

  • SD BIOSENSOR INC. CORÉIA DO SUL

Other registrations held by DESCARPACK DESCARTAVEIS DO BRASIL LTDAview all

MÁSCARA N95 / PFF2 DESCARPACK

10330660022

Torneira 3 vias Descarpack

10330660036

SAPATILHAS PROPÉ DESCARTÁVEIS DESCARPACK II

10330660041

SERINGA DESCARTÁVEL DESCARPACK COM AGULHA - LIFELONG

10330660046

AGULHA DESCARTÁVEL DESCARPACK I

10330660047

COMPRESSA PARA CAMPO OPERATÓRIO NÃO ESTÉRIL DESCARPACK II

10330660048

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