International safety notice
Corrective action on volumetric infusion pumps Volumed μVP7000 from Arcomed
Germany / BfArM · DEU · Sep 19, 2005
Key facts
| Title | Corrective action on volumetric infusion pumps Volumed μVP7000 from Arcomed |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Corrective action on volumetric infusion pumps Volumed μVP7000 from Arcomed |
| Manufacturer | Corrective action on volumetric infusion pumps Volumed μVP7000 from Arcomed |
| Models | ΜVP7000, 03.08.05 |
| Date | Sep 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