International safety notice
Software Upgrade required on DigitalDiagnost X-ray systems with software versions 2.0.2 und 2.1.3, Philips Medical Systems
Germany / BfArM · DEU · Nov 29, 2012
Key facts
| Title | Software Upgrade required on DigitalDiagnost X-ray systems with software versions 2.0.2 und 2.1.3, Philips Medical Systems |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Software Upgrade required on DigitalDiagnost X-ray systems with software versions 2.0.2 und 2.1.3, Philips Medical Systems |
| Manufacturer | Software Upgrade required on DigitalDiagnost X-ray systems with software versions 2.0.2 und 2.1.3, Philips Medical Systems |
| Models | FSN-71200061, 2.1.4, 1-800-722-9377, 06094, FCO-71200087, 06096, 2.0.2, 83902, 06095, FSN-71200087, 2.0.2SP1, 2.1.3 |
| Date | Nov 29, 2012 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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