357 results
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37ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Injury
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COROMETRIC FETAL ECG CABLE
FDA Adverse Event
Injury
·GE MEDICAL SYSTEMS·Product code KXN·April 16, 2007
DISPOSABLE SENSOR
FDA Adverse Event
Injury
·CRITICARE SYSTEMS, INC.·Product code KXN·May 10, 1993
FETAL HEART MONITOR
FDA Adverse Event
Injury
·PHILLIPS MEDICAL SYSTEMS·Product code KXN·November 6, 2001
(QS) COROMETRICS/GE MEDICAL
FDA Adverse Event
Injury
·G.E. MEDICAL SYSTEMS, INFO TECH SYSTEMS·Product code KXN·November 5, 2001
LUNDIA K 5N
FDA Adverse Event
Injury
·CGH·Product code KDI·October 14, 1993
UNKNOWN T2 KNEE ARTHRODESIS NAIL (T2 KAN)
FDA Adverse Event
Injury
·STRYKER GMBH·Product code HSB·January 16, 2025
UNKNOWN T2 KNEE ARTHRODESIS NAIL (T2 KAN)
FDA Adverse Event
Injury
·STRYKER GMBH·Product code HSB·January 16, 2025
UNKNOWN T2 KNEE ARTHRODESIS NAIL (T2 KAN)
FDA Adverse Event
Injury
·STRYKER GMBH·Product code HSB·January 16, 2025
UNKNOWN T2 KNEE ARTHRODESIS NAIL (T2 KAN)
FDA Adverse Event
Injury
·STRYKER GMBH·Product code HSB·January 16, 2025
UNKNOWN T2 KNEE ARTHRODESIS NAIL (T2 KAN)
FDA Adverse Event
Injury
·STRYKER GMBH·Product code HSB·January 16, 2025
UNKNOWN T2 KNEE ARTHRODESIS NAIL (T2 KAN)
FDA Adverse Event
Injury
·STRYKER GMBH·Product code HSB·January 15, 2025
SYSMEX XN-10
FDA Adverse Event
Injury
·SYSMEX CORPORATION·Product code GKZ·April 1, 2016
TIMAX
FDA Adverse Event
Injury
·NSK TOCHIGI-KEN·Product code EGS·March 25, 2010
TIMAX
FDA Adverse Event
Injury
·NSK TOCHIGI-KEN·Product code EGS·December 31, 2009
TIMAX
FDA Adverse Event
Injury
·NSK TOCHIGI-KEN·Product code EGS·December 31, 2009
TIMAX
FDA Adverse Event
Injury
·NSK TOCHIGI-KEN·Product code EGS·December 31, 2009
TIMAX
FDA Adverse Event
Injury
·NSK TOCHIGI-KEN·Product code EGS·June 20, 2011
SURGIC XT
FDA Adverse Event
Injury
·NSK TOCHIGI-KEN·Product code EBW·September 24, 2010
TIMAX
FDA Adverse Event
Injury
·NSK TOCHIGI-KEN (JAPAN)·Product code EGS·June 8, 2010
TIMAX
FDA Adverse Event
Injury
·NSK TOCHIGI-KEN (JAPAN)·Product code EGS·October 15, 2009