7 results
·
39ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
SALUTE FIXATION DEVICE
FDA Adverse Event
Malfunction
·DAVOL INC., SUB. C.R. BARD, INC.·Product code GDW·March 17, 2005
PALAXPRESS, CLEAR, 1000G POWDER
FDA Adverse Event
Injury
·HERAEUS KULZER GMBH & CO. KG, MEDICAL DIVISION·Product code EBI·February 1, 2012
U BY KOTEX SLEEK
FDA Adverse Event
Malfunction
·K-C AFC MANUFACTURING, S. DE R.L. DE C.V·Product code HEB·August 31, 2018
EON MINI
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 10, 2013
REAMER
FDA Adverse Event
Malfunction
·SYNTHES (USA)·Product code HTO·September 24, 2014
VS3: NBP, SP02, TEMP
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code MHX·May 25, 2011
U BY KOTEX SLEEK
FDA Adverse Event
Malfunction
·K-C AFC MANUFACTURING, S. DE R.L. DE C.V·Product code HEB·June 27, 2018