554 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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THORATEC® HEARTMATE 3® LVAS IMPLANT KIT
FDA Adverse Event
Death
·THORATEC CORPORATION·Product code DSQ·November 29, 2023
INTRA AORTIC BALLON PUMP
FDA Adverse Event
Injury
·MAQUET CARDIOVASCULAR US SALES LLC / DATASCOPE CORP.·Product code DSP·September 7, 2021
GENTEC®
FDA UDI
GENTEC(SHANGHAI)CORPORATION·06970966661543·882VR series suction regulator is a suction reg...
GENTEC®
FDA UDI
GENTEC(SHANGHAI)CORPORATION·06970966661185·881VR series suction regulator is a dual purpos...
GENTEC®
FDA UDI
GENTEC(SHANGHAI)CORPORATION·06970966660751·881VR series suction regulator is a dual purpos...
GENTEC®
FDA UDI
GENTEC(SHANGHAI)CORPORATION·06970966661635·882VR series suction regulator is a suction reg...
GENTEC®
FDA UDI
GENTEC(SHANGHAI)CORPORATION·06970966661970·882VR series suction regulator is a suction reg...
GENTEC®
FDA UDI
GENTEC(SHANGHAI)CORPORATION·06970966660287·881VR series suction regulator is a dual purpos...
GENTEC®
FDA UDI
GENTEC(SHANGHAI)CORPORATION·06970966662397·882VR series suction regulator is a suction reg...
GENTEC®
FDA UDI
GENTEC(SHANGHAI)CORPORATION·06970966660928·881VR series suction regulator is a dual purpos...
GENTEC®
FDA UDI
GENTEC(SHANGHAI)CORPORATION·06970966661857·882VR series suction regulator is a suction reg...
THORATEC® HEARTMATE 3® LVAS IMPLANT KIT
FDA Adverse Event
Death
·THORATEC CORPORATION·Product code DSQ·November 14, 2024
Mod. UDPF powder w/o HT,Fe citrate -20kg
FDA UDI
Lonza Verviers·05407010124187·
HEARTMATE II LVAS
FDA Adverse Event
Death
·THORATEC CORPORATION·Product code DSQ·February 2, 2015
HEARTMATE II LEFT VENTRICULAR ASSIST DEVICE
FDA Adverse Event
Injury
·THORATEC CORP.·Product code DSQ·August 13, 2014
MEGA 8FR. 50CC IAB
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - FAIRFIELD·Product code DSP·October 19, 2021
MEGA 8FR. 50CC IAB
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - FAIRFIELD·Product code DSP·October 19, 2021
XEN 45 GTS
FDA Adverse Event
Injury
·ALLERGAN (IRVINE)·Product code KYF·January 31, 2023
HEARTMATE II LVAS
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·August 5, 2015
IMPELLA RP FLEX
FDA Adverse Event
Death
·ABIOMED, INC.·Product code PYX·December 10, 2025