International safety notice
Product corrective action for FC 500 flow cytometry systems with CXP software, Beckman Coulter
Germany / BfArM · DEU · Aug 15, 2006
Key facts
| Title | Product corrective action for FC 500 flow cytometry systems with CXP software, Beckman Coulter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | FC 500 flow cytometry systems with CXP software, Beckman Coulter |
| Manufacturer | Product corrective action for FC 500 flow cytometry systems with CXP software, Beckman Coulter |
| Models | 6CO$OR.PRO, 5COI0F&PRO, 00002334, 5COTOR.PRO, 526-7694, 6COIOR.PRO, 00002, 6COÄOR, 00002967, 6E€A0F.PRO, 147TH, 69015 and 3 more |
| Date | Aug 15, 2006 |
| 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