11 results
·
38ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
TUFF TT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·May 14, 2025
TUFF TT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·May 14, 2025
CS300 INTRA-AORTIC BALLOON PUMP, ENGLISH, 220V
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·July 14, 2025
CS100 INTRA-AORTIC BALLOON PUMP, FRENCH, 220V
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·October 30, 2023
AEQUALIS REVERSED CEMENTLESS METAPHYSIS HA D.36MM
FDA Adverse Event
Injury
·TORNIER S.A.S.·Product code KWS·May 30, 2023
IMPAX CV REPORTING
FDA Adverse Event
Malfunction
·AGFA HEALTHCARE CORP.·Product code LLZ·February 26, 2013
SYNCHRON® CX3 DELTA CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JGS·February 24, 2011
GENTLEPOWER LUX CONTRA ANGLE 25LPA
FDA Adverse Event
Injury
·KALTENBACH & VOIGT GMBH·Product code EKK·February 22, 2008
CS300 INTRA-AORTIC BALLOON PUMP, ENGLISH, 110V
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - MAHWAH·Product code DSP·July 21, 2022
AEQUALIS REVERSED GLENOSPHERE 10 DEGREES TILTED 36 MM X 25MM
FDA Adverse Event
Injury
·TORNIER S.A.S.·Product code KWS·April 25, 2022
AEQUALIS REVERSED CEMENTLESS METAPHYSIS HA D.36MM
FDA Adverse Event
Injury
·TORNIER S.A.S.·Product code KWS·April 20, 2023