International safety notice
Software Update for all VISULAS 532s VITE systems, Carl Zeiss Meditec
Germany / BfArM · DEU · May 17, 2010
Key facts
| Title | Software Update for all VISULAS 532s VITE systems, Carl Zeiss Meditec |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | all VISULAS 532s VITE systems, Carl Zeiss Meditec |
| Manufacturer | Software Update for all VISULAS 532s VITE systems, Carl Zeiss Meditec |
| Models | 624536900, 07745, DE55298748, 220-0, 2820800000343424200, 51•52, DE31820400000258072800, 258072800, 4.1.1, DE90820700000624S36900, 205623, 343424200 |
| Date | May 17, 2010 |
| 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