International safety notice
Update for the Instructions of Use (IFU) and Clinical Use Information for the Parachute Implant System, CardioKinetix
Germany / BfArM · DEU · Apr 23, 2015
Key facts
| Title | Update for the Instructions of Use (IFU) and Clinical Use Information for the Parachute Implant System, CardioKinetix |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Parachute Implant System, CardioKinetix |
| Manufacturer | Update for the Instructions of Use (IFU) and Clinical Use Information for the Parachute Implant System, CardioKinetix |
| Models | LPDS68, PC-2015-0004, PDS68, RPGC35, PGC68, PGC35, RPGC68, 364-7016, 09-APR-2015, RPGC92, PGC92 |
| Date | Apr 23, 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