International safety notice
Safety Notice for SynchroMed II Implantable Drug Infusion Pump - Model 8637, Medtronic
Germany / BfArM · DEU · Jul 22, 2009
Key facts
| Title | Safety Notice for SynchroMed II Implantable Drug Infusion Pump - Model 8637, Medtronic |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | SynchroMed II Implantable Drug Infusion Pump - Model 8637, Medtronic |
| Manufacturer | Safety Notice for SynchroMed II Implantable Drug Infusion Pump - Model 8637, Medtronic |
| Models | 31-45 |
| Date | Jul 22, 2009 |
| 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