ANVISA registration

Dry Fluorescence Immunoassay Analyzer

Registration 80105220325. Instrumento destinado a imunoensaios

Registration details

Registration number80105220325
Application number25351144506202618
Technical nameInstrumento destinado a imunoensaios
Risk classII
Published on21/09/2026
ValidityIndefinite validity

Registration holder

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

Manufacturer

  • DIYALAB ZJG BIOTECH CO., LTD CHINA, REPÚBLICA POPULAR

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