3 results
·
15ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
E SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·May 26, 2011
4 MOTOR ADVANCE BED
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·August 15, 2008
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·March 14, 2016