International safety notice
In vitro diagnostic kit
Brazil / Anvisa · BRA · Aug 12, 2013
Key facts
| Title | In vitro diagnostic kit |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | PSA IMMULITE / IMMULITE 1000 e PSA IMMULITE 2000 - Registro ANVISA Nº 10345160687 e 10345160915 |
| Manufacturer | SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD REINO UNIDO |
| Models | 10345160915, 10345160687 |
| Date | Aug 12, 2013 |
| 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