International safety notice
Medtronic SynchroMed II Implantable Drug Infusion Pumps - pumba mootor võib ootamatult seiskuda selles oleva võõrkeha tõttu
Estonia / EMDDB · EST · Oct 1, 2019
Key facts
| Title | Medtronic SynchroMed II Implantable Drug Infusion Pumps - pumba mootor võib ootamatult seiskuda selles oleva võõrkeha tõttu |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Medtronic SynchroMed II Implantable Drug Infusion Pumps |
| Manufacturer | MEDTRONIC SYNCHROMED II IMPLANTABLE DRUG INFUSION PUMPS |
| Models | 30-SEP-2019, 8637-40, 8637-20, FA889, 2018-05-04, 05APRIL-2019, 04-MAY-2018, 2019-04-05 |
| Date | Oct 1, 2019 |
| Regulator page | terviseamet.ee |
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