340 results
·
50ms
·
Sources: EU EUDAMED, US FDA
HEWLETT-PACKARD/AGILENT TECHNOLOGIES
FDA Adverse Event
Other
·AGILENT TECHNOLOGIES, INC.·Product code MLN·June 21, 2001
HEWLETT PACKARD CO
FDA Adverse Event
Malfunction
·HEWLETT PACKARD·Product code LDD·February 12, 1997
HEWLETT PACKARD CO.
FDA Adverse Event
Malfunction
·HEWLETT PACKARD CO./MEDICAL PROPERTY DIVISION·Product code LDD·March 4, 1998
GOLD THERMODILUTION CATHETER
FDA Adverse Event
Malfunction
·VIGGO SPECTROMED·Product code KRB·July 29, 1992
HEWLETT PACKARD (NOW PHILLIPS)-"MOR
FDA Adverse Event
Death
·*·Product code DRT·November 12, 2002
OMNICARE COMNPONENT MINITORING SYSTEM
FDA Adverse Event
Death
·HEWLETT-PACKARD CO.·Product code DRT·September 4, 1996
CODEMASTER XL+
FDA Adverse Event
Death
·HEWLETT-PACKARD CO·Product code LDD·September 26, 1996
CODE MASTER XL+
FDA Adverse Event
Death
·HEWLETT PACKARD CO·Product code LDD·September 26, 1996
M2360A
FDA Adverse Event
Death
·HEWLETT-PACKARD CO·Product code MHX·September 24, 1996
HEWLETT PACKARD TELEMETRY
FDA Adverse Event
Death
·HEWLETT PACKARD CO.·Product code DRG·September 14, 1996
HEWLETT PACKARD DISPOSABLE SPIRAL ELECTRODE FOR FETAL MONITR
FDA Adverse Event
Injury
·HEWLETT-PACKARD CO·Product code HGP·July 1, 1996
MONITOR/DEFIBRILLATOR/PACING PAD
FDA Adverse Event
Malfunction
·HEWLETT-PACKARD CO.·Product code LDD·September 6, 1996
21363A BIPLANE TEE PROBE
FDA Adverse Event
Injury
·HEWLETT-PACKARD CO.·Product code IYO·September 25, 1996
78720A ARRHYTHMIA MONITORING SYSTEM
FDA Adverse Event
Death
·HEWLETT-PACKARD CO·Product code DRT·September 6, 1996
INTERNAL RACK
FDA Adverse Event
Injury
·HEWLETT-PACKARD CO.·Product code MOY·September 24, 1996
78100A TELEMETRY MONITOR
FDA Adverse Event
Death
·HEWLETT-PACKARD CO.·Product code DRT·September 5, 1996
DEFIBRILLATOR
FDA Adverse Event
Malfunction
·HEWLETT-PACKARD CO.·Product code LDD·July 15, 1996
CODEMASTER XL+
FDA Adverse Event
Death
·HEWLETT PACKARD CO.·Product code LDD·January 22, 2004
TELEMETRY TRANSMITTER
FDA Adverse Event
Death
·HEWLETT-PACKARD CO.·Product code DRT·April 1, 1996
CENTRAL MONITOR SYSTEM
FDA Adverse Event
Death
·HEWLETT PACKARD CO.·Product code DRT·June 19, 1996