International safety notice
In Vitro Diagnostic Kit
Brazil / Anvisa · BRA · Sep 3, 2013
Key facts
| Title | In Vitro Diagnostic Kit |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | PSA Third Generation IMMULITE®/ IMMULITE® 1000 - Registration 10345160987 Lots: 320 and 321. |
| Manufacturer | SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS |
| Models | 10345160987 |
| Date | Sep 3, 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