7 results
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21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
PREMIER ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC, INC.·Product code KWQ·August 12, 2011
PREMIER® ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·March 3, 2017
PREMIER® ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·March 3, 2017
PREMIER® ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 7, 2015
PMO COMBINED PROBE CONTAINING BOTH OXYGEN AND TE
FDA Adverse Event
Malfunction
·GMS·Product code DRF·November 11, 2010
OXIMAX N-560 PULSE OXIMETER
FDA Adverse Event
Malfunction
·MEDIANA·Product code DQA·March 4, 2014
DEXTRUS 4136
FDA Adverse Event
Malfunction
·BIOTRONIK SE & CO. KG·Product code NVZ·December 27, 2012