International safety notice
Corrective action for Coulter UniCel DxI, Beckman Coulter
Germany / BfArM · DEU · Dec 23, 2004
Key facts
| Title | Corrective action for Coulter UniCel DxI, Beckman Coulter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Coulter UniCel DxI, Beckman Coulter |
| Manufacturer | Corrective action for Coulter UniCel DxI, Beckman Coulter |
| Models | 443-4848, 34401, 01-123456M, 553181084, 23456, PFI0$, 34222, 1-800, 34292, 2-0.1, 854-3633 |
| Date | Dec 23, 2004 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 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