International safety notice
Safety Notice for VISALIS S500 and VISALIS V500, Carl Zeiss Meditec AG
Germany / BfArM · DEU · Oct 1, 2012
Key facts
| Title | Safety Notice for VISALIS S500 and VISALIS V500, Carl Zeiss Meditec AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | VISALIS S500 and VISALIS V500, Carl Zeiss Meditec AG |
| Manufacturer | Safety Notice for VISALIS S500 and VISALIS V500, Carl Zeiss Meditec AG |
| Models | 20.06.2012, 07745, 220-0, 624536900, 51-52, 07740, 205623, 20-2035, 8EXXX, DE55298748, 303043-9901-000, DE31820400000258072800 and 3 more |
| Date | Oct 1, 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