International safety notice
Diagnostické zdravotnické prostředky in vitro
Czech / Ksrzis · CZE · Oct 29, 2018
Key facts
| Title | Diagnostické zdravotnické prostředky in vitro |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | Lactate Dehydrogenase Flex reagent cartridge (Reagenční kazeta Lactate Dehydrogenase (LDI) Flex®) |
| Manufacturer | Siemens Healthcare Diagnostics Inc., USA |
| Models | 18106BC, K2054, 19714-6101, 10464323, 18240BA, 18036BC, VC-18-07.A.OUS, VC-18-07, 17342BA, 18162AC, K2054KAT, 18199BA and 3 more |
| Event type | Safety Notice |
| Date | Oct 29, 2018 |
| Regulator page | eregpublicsecure.ksrzis.cz |
At a glance
- No Recall
- Yes 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