ANVISA registration

Covid-19 Ag Rapid Test (Oral Fluid)

Registration 10009010371. CORONAVÍRUS

Registration details

Registration number10009010371
Application number25351469594202153
Technical nameCORONAVÍRUS
Risk classIII
Published on31/05/2021
ValidityValid until 31/05/2031

Registration holder

Legal nameLABTEST DIAGNOSTICA S/A
CNPJ16.516.296/0001-38

Manufacturer

  • LABTEST DIAGNOSTICA S/A BRASIL

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GLICOSE PAP LIQUIFORM

10009010003

GAMA GT LIQUIFORM

10009010004

PADRAO DE BILIRRUBINA

10009010010

UREIA CE

10009010011

MAGNESIO

10009010012

CAPACIDADE DE LIGACAO DE FERRO

10009010013

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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