22 results · 27ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

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