International safety notice
Safety Corrective Action for the Hemofiltration Device AQUARIUS (regular platform 6), Nikkiso Deutschland GmbH
Germany / BfArM · DEU · Feb 7, 2014
Key facts
| Title | Safety Corrective Action for the Hemofiltration Device AQUARIUS (regular platform 6), Nikkiso Deutschland GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Hemofiltration Device AQUARIUS (regular platform 6), Nikkiso Deutschland GmbH |
| Manufacturer | Safety Corrective Action for the Hemofiltration Device AQUARIUS (regular platform 6), Nikkiso Deutschland GmbH |
| Models | 6.02.07, 20MMHG, 10MMHG, 30855, 2009-019-RN |
| Date | Feb 7, 2014 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 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