International safety notice
Diagnostické zdravotnické prostředky in vitro
Czech / Ksrzis · CZE · Aug 20, 2018
Key facts
| Title | Diagnostické zdravotnické prostředky in vitro |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | RAPIDPoint 405 Blood Gas Analyzer; RAPIDPoint 500 Blood Gas Analyzer; RAPIDLab 1245 Blood Gas Analyzer; RAPIDLab 1265 Blood Gas Analyzer |
| Manufacturer | Siemens Healthcare Diagnostics, Inc. |
| Models | 97.37, 10320055, 10314817, 15.24, 16.72, 10317193, 87.98, 10321844, 10328302, 16.27, 10336784, 18-010.A.OUS and 34 more |
| Event type | Safety Notice |
| Date | Aug 20, 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