International safety notice
Safety Notice for WaveLight® FS 200 Femtosecond Laser, Wave Light GmbH
Germany / BfArM · DEU · Apr 29, 2011
Key facts
| Title | Safety Notice for WaveLight® FS 200 Femtosecond Laser, Wave Light GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | WaveLight® FS 200 Femtosecond Laser, Wave Light GmbH |
| Manufacturer | Safety Notice for WaveLight® FS 200 Femtosecond Laser, Wave Light GmbH |
| Models | ABLETORESUMEKERATOPLASTYTREATMENTSWITHTHEWAVELIGHT®FS200, ONAPRIL8, CUTSFORKERATOPLASTYANDCORNEALHARVESTING.THISDEVICEMODIFICATIONAFFECTSWAVELIGHT®FS200, WAVELIGHT®FS200FEMTOSECONDLASER, THEWAVELIGHT®FS200SOFTWAREHASBEENUPGRADED, CAREPROFESSIONALSDISCONTINUEKERATOPLASTYCUTSWITHTHEWAVELIGHTFS200UNTILTHENEWSOFTWARE, FS200FEMTOSECONDLASERUSEDINREFRACTIVESURGERYFORCREATIONOFCORNEALFLAPS, USINGTHEWAVELIGHT®FS200FEMTOSECONDLASER.ADDITIONALLY, DEVICEMODIFICATIONFORTHEWAVELIGHT®FS200FEMTOSECONDLASER, DISPATCHEDTOYOURSITEWITHINTHENEXT48WEEKSTOINSTALLTHESOFTWAREVERSIONAFTERWHICHYOUWILLBE, THEOTHERFUNCTIONSOFTHEWAVELIGHTFS200 |
| Date | Apr 29, 2011 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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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