8 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
UNKNOWN DEPUY 52X28MM +4 LINER
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JDI·December 1, 2010
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE REHABILITATION EQUIP·Product code CAW·July 3, 2014
T-PAL LARGE TRIAL IMPLANT SIZ 7 NON DETA
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HSB·December 7, 2012
PINNACLE MTL INS NEUT36IDX54OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KWA·May 30, 2013
ARTICULEZE M HEAD 36MM -2
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·May 30, 2013
CORAIL2 STD SIZE 10
FDA Adverse Event
Injury
·DEPUY FRANCE SAS - 3003895575·Product code KWA·October 9, 2013
AGILIA VP MC WIFI AU
FDA Adverse Event
Malfunction
·FRESENIUS VIAL S.A.S.·Product code FRN·November 26, 2024
AGILIA VP MC WIFI AU
FDA Adverse Event
Malfunction
·FRESENIUS VIAL S.A.S.·Product code FRN·November 26, 2024