ANVISA registration

FASTLINE LEISHMANIA IgG/IgM

Registration 80105220183. LEISHMANIA SP

Registration details

Registration number80105220183
Application number25351843338202302
Technical nameLEISHMANIA SP
Risk classIII
Published on08/04/2024
ValidityValid until 08/04/2034

Registration holder

Legal nameKHAYROS DIAGNOSTICA FABRICACAO, COMERCIALIZACAO E DISTRIBUICAO DE PRODUTOS LTDA
CNPJ04.299.232/0001-43

Manufacturer

  • KHAYROS DIAGNOSTICA FABRICACAO, COMERCIALIZACAO E DISTRIBUICAO DE PRODUTOS LTDA BRASIL

Other registrations held by KHAYROS DIAGNOSTICA FABRICACAO, COMERCIALIZACAO E DISTRIBUICAO DE PRODUTOS LTDAview all

FR-IgG SORBENT SYM

80105220074

Tampão de Eluição para kits Q-PREVEN

80105220098

ZikV/DenV/ChikV Savyon

80105220105

LAMP COVID 19

80105220115

FASTLINE COVID-19 Ag

80105220116

DETECTA COVID

80105220117

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