International safety notice
DENGUE
Brazil / Anvisa · BRA · May 2, 2016
Key facts
| Title | DENGUE |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name of the product: TOYO DENGUE CASSETTE TEST KIT /// Registration number: 80721060014 /// Affected model(s): TDGP01/// affected batch: DG11403/// Product risk class: III. |
| Manufacturer | DETENTOR DO REGISTRO JC PHARMA HEALTH COMÉRCIO EXPORTAÇÃO E IMPORTAÇÃO LTDAMELTD CNPJ 01662176000171 RUA DIOGO VAZ N 45 CAMBUCI SÃO PAULO SP TELEFONE PARA SUPORTE 11 50715486 FABRICANTE TURKLAB TIBBI MALZEMELER SAN TIC AS ENDEREÇO IAOSB 10040 SOKAK NO20 35620 ÇIGLI TURQUIA |
| Models | DG11403, TDGP01, 80721060014 |
| Date | May 2, 2016 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1