21 results · 22ms · Sources: EU EUDAMED, US FDA

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DAN MONOPOLAR LAP ACCESSORIES

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

INSPECTRA TISSUE SPECTROMETER SYSTEM (INSPECTRA), MODEL 325

FDA 510(k)
FDA Class 2 ·Cardiovascular

OPTIMA MX

FDA 510(k)
FDA Class 1 ·Dental

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

FLEXTEND

FDA Adverse Event
Malfunction ·CPI - DEL CARIBE·Product code NVN·April 11, 2013

ASR ACETABULAR CUPS 50

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·April 7, 2011

FENESTRATED MARYLAND BIPOLAR INSTRUMENT

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL, INC.·Product code GEI·May 27, 2008

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