International safety notice
Follow-up Information for the SynchroMed® II Implantable Drug Infusion Pump, Medtronic
Germany / BfArM · DEU · May 7, 2015
Key facts
| Title | Follow-up Information for the SynchroMed® II Implantable Drug Infusion Pump, Medtronic |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the SynchroMed® II Implantable Drug Infusion Pump, Medtronic |
| Manufacturer | Follow-up Information for the SynchroMed® II Implantable Drug Infusion Pump, Medtronic |
| Models | FA649, 8637‐20, 8637‐40 |
| Date | May 7, 2015 |
| 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