International safety notice
Diagnostické zdravotnické prostředky in vitro
Czech / Ksrzis · CZE · Feb 26, 2018
Key facts
| Title | Diagnostické zdravotnické prostředky in vitro |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | IMMULITE®/IMMULITE® 1000 IMMULITE® 2000/IMMULITE® 2000 XPi metody |
| Manufacturer | Siemens Healthcare Diagnostics Products Limited |
| Models | 10380962, LKTY1, L2KCE2, IMC18-02.B.OUS, 10380948, L2KCE6, 10380945, 10487629, L2KFO2, 10380994, L2KG46, LKMB1 and 43 more |
| Event type | Safety Notice |
| Date | Feb 26, 2018 |
| Regulator page | eregpublicsecure.ksrzis.cz |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 Matching catalog numbers 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