ANVISA registration

Discriminatory Probe Reagent (Procleix ArboPlex Assay)

Registration 80134860313. CHIKUNGUNYA, DENGUE, FEBRE DO NILO OCIDENTAL E ZIKA

Registration details

Registration number80134860313
Application number25351453314202438
Technical nameCHIKUNGUNYA, DENGUE, FEBRE DO NILO OCIDENTAL E ZIKA
Risk classIV
Published on22/04/2025
ValidityValid until 22/04/2035

Registration holder

Legal nameGRIFOLS BRASIL LTDA
CNPJ02.513.899/0001-71

Manufacturer

  • GRIFOLS DIAGNOSTICS SOLUTIONS INC ESTADOS UNIDOS DA AMÉRICA

Other registrations held by GRIFOLS BRASIL LTDAview all

AUTOANALISADOR PARA IMUNOHEMATOLOGIA WADIANA COMPACT

10364120050

IDENTISERA DIANA

10364120056

SERASCAN DIANA 2P

10364120059

SERASCAN DIANA 4

10364120060

SERASCAN DIANA 4P

10364120062

IDENTISERA DIANA EXTEND P

10364120064

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