22 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
TEMPUS PRO
FDA Adverse Event
Malfunction
·REMOTE DIAGNOSTIC TECHNOLOGIES LTD.·Product code MHX·December 30, 2024
CS300
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·March 28, 2014
TRUSTEEL
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·November 7, 2024
TRUSTEEL
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·November 7, 2024
CS300 INTRA-AORTIC BALLOON PUMP, ENGLISH, 110V
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - MAHWAH·Product code DSP·May 25, 2023
CS300 INTRA-AORTIC BALLOON PUMP, ENGLISH, 220V
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·March 17, 2025
CS300
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - MAHWAH·Product code DSP·July 15, 2022
CS300 INTRA-AORTIC BALLOON PUMP, ENGLISH, 110V
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·November 25, 2025
CS300 INTRA-AORTIC BALLOON PUMP, ENGLISH, 110V
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - MAHWAH·Product code DSP·November 22, 2022
CS100
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·November 27, 2013
CS300
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·September 30, 2013
CS100 INTRA-AORTIC BALLOON PUMP, ENGLISH, 110V
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·February 20, 2025
CS300
FDA Adverse Event
Malfunction
·DATASCOPE CORP.,·Product code DSP·July 29, 2014
CS300 INTRA-AORTIC BALLOON PUMP, ENGLISH, 110V
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·November 1, 2024
CS100
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·April 25, 2014
CS300 INTRA-AORTIC BALLOON PUMP, SPANISH, 220V
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·February 18, 2025
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 13, 2013
LINE SET FOR AQUARIUS
FDA Adverse Event
Malfunction
·HAEMOTRONICS SPA·Product code FJK·February 24, 2011
ACRYSOF RESTOR
FDA Adverse Event
Other
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MFK·February 15, 2008
PATIENT INFORMATION CENTER IX
FDA Adverse Event
Death
·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code MHX·March 13, 2025