International safety notice
In vitro diagnostic
Brazil / Anvisa · BRA · Feb 26, 2015
Key facts
| Title | In vitro diagnostic |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | ADVIA CENTAUR PRGE in vitro diagnostic kit, Risk class II, Registration: 10345160327. Serial numbers: 42564268; |
| Manufacturer | DETENTOR DO REGISTRO SIEMENS HEALTHCARE DIAGNÓSTICOS LTDA CNPJ 01449930000190 ENDEREÇO AV MUTINGA 3800 7º ANDAR PIRITUBA SÃO PAULO FABRICANTE SIEMENS HEALTHCARE DIAGNOSTICS INC ENDEREÇO 511 BENEDICT AVENUE TARRYTOWN NEW YORK 105915097 ESTADOS UNIDOS |
| Models | 42590268, 42624268, 10345160327, 42564268, 43742268, 44847268, 43538268, 43834268, 42565268, 42621268 |
| Date | Feb 26, 2015 |
| 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