International safety notice
Medical Device Correction for HDI4000 Ultrasound Systems, Philips
Germany / BfArM · DEU · Sep 29, 2008
Key facts
| Title | Medical Device Correction for HDI4000 Ultrasound Systems, Philips |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | HDI4000 Ultrasound Systems, Philips |
| Manufacturer | Medical Device Correction for HDI4000 Ultrasound Systems, Philips |
| Models | HD14000 |
| Date | Sep 29, 2008 |
| 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