2,393 results · 24ms · Sources: EU EUDAMED, US FDA

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FETAL MONITOR 118

FDA Adverse Event
Malfunction ·GE MEDICAL SYSTEMS INFO TECHNOLOGIES·Product code KXN·October 17, 2003

COROMETRICS

FDA Adverse Event
Malfunction ·GE MEDICAL SYSTEMS/MARQUETTE·Product code KXN·September 22, 2000

KENDALL LIFE TRACE LEG PLATE CABLE

FDA Adverse Event
Malfunction ·KENDALL-LTP·Product code KXN·October 17, 2000

FETAL MONITOR

FDA Adverse Event
Malfunction ·COROMETRIC MEDICAL SYSTEMS, INC.·Product code KXN·October 28, 1994

*

FDA Adverse Event
Malfunction ·AGILENT TECHNOLOGIES·Product code KXN·February 9, 2001

AVALON FM30

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYS·Product code KXN·September 16, 2009

MASTER TERMINAL

FDA Adverse Event
Malfunction ·HEWLETT PACKARD·Product code KXN·July 20, 1992

MODEL 500 INFANT MONITOR

FDA Adverse Event
Malfunction ·COROMETRICS MEDICAL SYS. INC.·Product code KXN·January 22, 1998

MODEL 500EXL INFANT MONITOR

FDA Adverse Event
Malfunction ·COROMETRICS MEDICAL SYSTEMS, INC.·Product code KXN·January 29, 1998

AXIS

FDA Adverse Event
Malfunction ·OXFORD INSTRUMENTS - MEDICAL SYSTEMS DIV.·Product code KXN·March 10, 1999

TWINS CAPABLE FETAL MONITOR

FDA Adverse Event
Malfunction ·HEWLETT PACKARD CO.·Product code KXN·March 20, 1996

KENDALL

FDA Adverse Event
Malfunction ·KENDALL - LTP THE LUDLOW CO LP·Product code KXN·November 8, 2002

UNSPECIFIED BD¿ PEN NEEDLE

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FMI·June 19, 2023

AVANTI JXN-26

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code JQC·January 28, 2025

ROCHE OMNI S

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code CHL·March 9, 2018

TIMAX

FDA Adverse Event
Malfunction ·NSK TOCHIGI-KEN·Product code EGS·December 10, 2009

TIMAX

FDA Adverse Event
Malfunction ·NSK TOCHIGI-KEN·Product code EGS·December 31, 2008

TIMAX

FDA Adverse Event
Malfunction ·NSK TOCHIGI-KEN·Product code EGS·December 31, 2008

TIMAX

FDA Adverse Event
Malfunction ·NSK TOCHIGI-KEN·Product code EGS·December 31, 2008

TI MAX

FDA Adverse Event
Malfunction ·NSK TOCHIGI-KEN·Product code EGS·December 31, 2008