ANVISA registration

FASTLINE MYCOPLASMA Ag

Registration 80105220155. MYCOPLASMA

Registration details

Registration number80105220155
Application number25351238415202308
Technical nameMYCOPLASMA
Risk classIII
Published on11/12/2023
ValidityValid until 11/12/2033

Registration holder

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

Manufacturer

  • HANGZHOU ALLTEST BIOTECH CO. LTD CHINA, REPÚBLICA POPULAR

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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.

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