International safety notice
Diagnostické zdravotnické prostředky in vitro
Czech / Ksrzis · CZE · Feb 5, 2020
Key facts
| Title | Diagnostické zdravotnické prostředky in vitro |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | IMMULITE® / IMMULITE® 1000 Progesterone/ IMMULITE® 2000 / IMMULITE® 2000 XPi Progesteron, |
| Manufacturer | Siemens Healthcare Diagnostics Products Limited, GB |
| Models | 19-07, IMC19-07.B.OUS, IMC19-07.A.US, 2018-10-19, 19-07B, 2018-09-28, 10381128, LKPW1, 10381181, 01-6297401, 10591, 10381170 and 7 more |
| Event type | Safety Notice |
| Date | Feb 5, 2020 |
| 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