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ANVISA registration 80524900081Valid until Apr 22, 2036

COMBINED PARAMETERS IN THE SAME PRODUCT - CLASS III

ANVISA Registration Number: 80524900081BIO ADVANCE DIAGNOSTICOS LTDACTK BIOTECH, INC.Risk Class III
Device names
Technical name
COMBINED PARAMETERS IN THE SAME PRODUCT - CLASS III
PT: PARÂMETROS COMBINADOS NO MESMO PRODUTO - CLASSE III
Commercial name
Teste Rápido OnSite COVID-19 + Influenza A/B Ag
Risk class
Class III
Registration details
Registration Number
80524900081
Process Number
25351016503202695
CNPJ
09593438000103
Company information
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Apr 22, 2026
Validity
22/04/2036
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for COMBINED PARAMETERS IN THE SAME PRODUCT - CLASS III in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80524900081 and manufactured by CTK BIOTECH, INC.. The registration is held by BIO ADVANCE DIAGNOSTICOS LTDA with validity until Apr 22, 2036.

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.