20 results · 32ms · Sources: EU EUDAMED, US FDA

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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