International safety notice
Safety Notice concerning the FreeSpan™ Traverse and FreeSpan Ultra Twin™ Traverse, Liko AB
Germany / BfArM · DEU · Sep 11, 2012
Key facts
| Title | Safety Notice concerning the FreeSpan™ Traverse and FreeSpan Ultra Twin™ Traverse, Liko AB |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Safety Notice concerning the FreeSpan™ Traverse and FreeSpan Ultra Twin™ Traverse, Liko AB |
| Manufacturer | Safety Notice concerning the FreeSpan™ Traverse and FreeSpan Ultra Twin™ Traverse, Liko AB |
| Models | 500-1621, 3103015, 3EN110750-07, 174446, 3101507, 4420-4930, 3101802-06, 3101554-58, 3101703, 600-1896, 3101165-68, 3126008 and 52 more |
| Date | Sep 11, 2012 |
| 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