25 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
STRYKER DISCMONITOR
FDA 510(k)
FDA Class 2
·General Hospital
DEROYAL SURGICAL, UMBILICUP
FDA 510(k)
FDA Class 2
·Hematology
CORDIS 13F CATHETER SHEATH INTRODUCER
FDA 510(k)
FDA Class 2
·Cardiovascular
BIPAP AUTO M-SERIES
FDA Adverse Event
Death
·RESPIRONICS, INC·Product code BZD·July 11, 2012
BIPAP AUTO SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 9, 2022
BIPAP AUTO SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 14, 2022
BIPAP AUTO BIFLEX
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 14, 2022
BIPAP AUTO SERIES ASSY
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 31, 2022
BIPAP AUTO SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 14, 2022
BIPAP AUTO SERIES ASSY
FDA Adverse Event
Malfunction
·RESPIRONICS, INC·Product code BZD·March 31, 2022
BIPAP AUTO SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 9, 2022
BIPAP AUTO SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 9, 2022
BIPAP AUTO SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 9, 2022
BIPAP AUTO SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 31, 2022
FLEXTOME? CUTTING BALLOON?
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - GALWAY·Product code LOX·April 10, 2013
RIATA ST ACTIVE FIXATION LEAD
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 27, 2008
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·April 12, 2011
BIPAP AUTO M-SERIES
FDA Adverse Event
Other
·RESPIRONICS INC.·Product code BZD·June 8, 2012
BIPAP AUTO M-SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·May 20, 2011
REMSTAR BIPAP AUTO M-SERIES
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·August 27, 2010