20 results
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32ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
SOVEREIGN SPINAL SYSTEM
FDA Adverse Event
Injury
·MSD DEGGENDORF MFG·Product code MAX·December 23, 2014
SOVEREIGN SPINAL SYSTEM
FDA Adverse Event
Injury
·MSD DEGGENDORF MFG·Product code MAX·November 22, 2014
SOVEREIGN SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MSD DEGGENDORF MFG·Product code OVD·April 21, 2018
WALLFLEX ESOPHAGEAL
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code ESW·January 23, 2025
SOVEREIGN SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH·Product code MAX·May 10, 2013
SOVEREIGN SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MDT SWINNEA DC·Product code MAX·February 18, 2011
SOVEREIGN SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MSD DEGGENDORF MFG·Product code OVD·August 9, 2017
PROMOTE RF CRT-D
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL INC., CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·January 13, 2014
GAS MODULE II
FDA Adverse Event
Malfunction
·MINDRAY DS USA, INC.·Product code BZK·April 30, 2013
UNICEL® DXC 800 PRO SYNCHRON® CHEMISTRY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·May 17, 2011
SOVEREIGN¿ SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH·Product code MAX·November 15, 2012
SOVEREIGN SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MSD DEGGENDORF MFG·Product code OVD·November 28, 2017
SOVEREIGN SPINAL SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code MAX·August 19, 2011
WALLFLEX ESOPHAGEAL
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code ESW·February 14, 2025
SOVEREIGN SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MSD DEGGENDORF MFG·Product code OVD·November 30, 2015
SOVEREIGN¿ SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH·Product code MAX·December 5, 2012
SOVEREIGN¿ SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MSD DEGGENDORF MFG·Product code OVD·November 18, 2025
PROXIMAL HUMERUS, RIGHT, LONG, 7X200MM
FDA Adverse Event
Injury
·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code HSB·September 25, 2023
INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR
FDA Adverse Event
Injury
·MSD DEGGENDORF MFG·Product code OVD·December 18, 2019
BLUNT TIP SCREW, 4X36MM
FDA Adverse Event
Injury
·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code HSB·September 25, 2023