International safety notice
Products for in vitro diagnostic use
Brazil / Anvisa · BRA · Feb 8, 2018
Key facts
| Title | Products for in vitro diagnostic use |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Laboratory tests that use assay methodologies with Biotin technology to promote the connection with specific protein biomarkers. |
| Manufacturer | O ALERTA DE SEGURANÇA EM TECNOVIGILÂNCIA ALERTA 2482 NÃO É RELACIONADO A UM PRODUTO ESPECÍFICO MAS APLICASE A DIVERSAS METODOLOGIAS DE ENSAIO CUJOS TESTES UTILIZAM TECNOLOGIA COM BIOTINA PARA PROMOVER A LIGAÇÃO COM BIOMARCADORES DE PROTEÍNAS ESPECÍFICOS |
| Date | Feb 8, 2018 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
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