3 results
·
35ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Recall
×
Electric Wheelchairs: a) C300 CORPUS II b) C350 CORPUS II c) C400 CORPUS II d) C400 CORPUS II LR e) C500 CORPUS II f) C500 CORPUS II LR
FDA Recall
Terminated
·Permobil, Ab Arvaltsvagen 10·Product code ITI·September 1, 2017
Electric Wheelchair bases: a) C300 b) C350 c) C400 d) C500
FDA Recall
Terminated
·Permobil, Ab Arvaltsvagen 10·Product code ITI·September 1, 2017
Permobil powered wheelchairs, Model Numbers: (a) M300 PS, (b) C300 PS, (c) C350 PS, (d) C500 PS, (e) C400 PS Product Usage: The devices identified are intended to provide outdoor and indoor mobility to persons limited to a seated position that can operate a powered wheelchair.
FDA Recall
Terminated
·Permobil, Ab Arvaltsvagen 10·Product code ITI·August 15, 2018