International safety notice
Safety Notice for MX 8000 IDT 16, Philips
Germany / BfArM · DEU · Sep 2, 2010
Key facts
| Title | Safety Notice for MX 8000 IDT 16, Philips |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | MX 8000 IDT 16, Philips |
| Manufacturer | Safety Notice for MX 8000 IDT 16, Philips |
| Models | V4.2.1, 4X4.5, 1-800-7229377 |
| Date | Sep 2, 2010 |
| 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