25 results · 28ms · Sources: EU EUDAMED, US FDA

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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