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ANVISA registration 80020690418Valid until Sep 13, 2031

ANTIGEN AND ANTIBODY TO HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, TYPE 2 AND TYPE 1 SUBGROUP O (HIV)

ANVISA Registration Number: 80020690418BIO-RAD LABORATORIOS BRASIL LTDABIO-RADRisk Class IV
Device names
Technical name
ANTIGEN AND ANTIBODY TO HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, TYPE 2 AND TYPE 1 SUBGROUP O (HIV)
PT: ANTÍGENO E ANTICORPO DO VÍRUS DA IMUNODEFICIÊNCIA HUMANA ADQUIRIDA TIPO 1, TIPO 2 E TIPO 1 SUBGRUPO O (HIV)
Commercial name
Família Access HIV combo V2
Risk class
Class IV
Registration details
Registration Number
80020690418
Process Number
25351490255202136
CNPJ
03188198000177
Company information
Manufacturer
BIO-RAD
Manufacturing Country
France
PT: FRANÇA
Dates and status
Publication Date
Sep 13, 2021
Validity
13/09/2031
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for ANTIGEN AND ANTIBODY TO HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, TYPE 2 AND TYPE 1 SUBGROUP O (HIV) in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80020690418 and manufactured by BIO-RAD. The registration is held by BIO-RAD LABORATORIOS BRASIL LTDA with validity until Sep 13, 2031.

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