International safety notice
Safety Notice for TheraScreen® K-RAS Mutation Kit, QIAGEN Manchester Ltd.
Germany / BfArM · DEU · Nov 24, 2010
Key facts
| Title | Safety Notice for TheraScreen® K-RAS Mutation Kit, QIAGEN Manchester Ltd. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | TheraScreen® K-RAS Mutation Kit, QIAGEN Manchester Ltd. |
| Manufacturer | Safety Notice for TheraScreen® K-RAS Mutation Kit, QIAGEN Manchester Ltd. |
| Models | KR-21, OFTH1S, DK241-OL, VR-2010-OOL, DK241, DK241-01, CUSTOMERS4, 29-13360, 13360, VR-2010-001, 05366216190, DK24J-OJ |
| Date | Nov 24, 2010 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No 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