International safety notice
Diagnostické zdravotnické prostředky in vitro
Czech / Ksrzis · CZE · Aug 12, 2015
Key facts
| Title | Diagnostické zdravotnické prostředky in vitro |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | Dade Actin Activated Cephaloplastin Reagent |
| Manufacturer | Siemens Healthcare Diagnostics Products GmbH |
| Models | BR06215, 557131, 557135, 557139A, 557134, 10445709, 557116, 557142, 10445709KAT, BR-06215, 557133, 557128 and 21 more |
| Event type | Safety Notice |
| Date | Aug 12, 2015 |
| Regulator page | eregpublicsecure.ksrzis.cz |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models 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