International safety notice
Corrective action for NIHON KOHDEN Electrocardiographs series "cardiofax m" ECG-2350, NIHON KOHDEN Europe GmbH
Germany / BfArM · DEU · Jul 14, 2014
Key facts
| Title | Corrective action for NIHON KOHDEN Electrocardiographs series "cardiofax m" ECG-2350, NIHON KOHDEN Europe GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | NIHON KOHDEN Electrocardiographs series "cardiofax m" ECG-2350, NIHON KOHDEN Europe GmbH |
| Manufacturer | Corrective action for NIHON KOHDEN Electrocardiographs series "cardiofax m" ECG-2350, NIHON KOHDEN Europe GmbH |
| Models | 01-05, 2350K, D-61191, 01-04, 20141, 01-07, ECG-2350, 01-03, D-14532, 573-19, 827-5, 114193 and 5 more |
| Date | Jul 14, 2014 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 Matching catalog numbers in FDA data
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