International safety notice
Corrective action from Agen BioMedical, BioMerieux and Behnk Elektronik for Compact X, Compact XR and Combi Systems
Germany / BfArM · DEU · Aug 19, 2005
Key facts
| Title | Corrective action from Agen BioMedical, BioMerieux and Behnk Elektronik for Compact X, Compact XR and Combi Systems |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Compact X, Compact XR and Combi Systems |
| Manufacturer | Corrective action from Agen BioMedical, BioMerieux and Behnk Elektronik for Compact X, Compact XR and Combi Systems |
| Models | Ⅱ4&니헓亡1, ΙΙΟΗΕ.ΙΘΙΙΘ9, •《기61.U, 이L꾜에0래D, &88工문。, 설월혈舅통磊응청경청8듄88유운운경, ΘΙΙΘ2ΦΟΙΩ•ΙΕΙ.ΙΙΒΜΟ |
| Date | Aug 19, 2005 |
| 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