10 results
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19ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
OLYMPUS
FDA Adverse Event
Malfunction
·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code FDF·September 12, 2008
OSTEO-SITE BONE BIOPSY NEEDLE
FDA Adverse Event
Malfunction
·COOK INC·Product code KNW·July 18, 2019
OSTEO-SITE BONE BIOPSY NEEDLE
FDA Adverse Event
Malfunction
·COOK INC·Product code KNW·June 17, 2019
PINNACLE MTL INS NEUT36IDX54OD
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS INC US·Product code KWA·March 3, 2014
ARTICULEZE M HEAD 36MM +8.5
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS INC US·Product code JDI·March 3, 2014
OSTEO-SITE BONE BIOPSY NEEDLE
FDA Adverse Event
Malfunction
·COOK INC·Product code KNW·January 23, 2019
OSTEO-SITE BONE BIOPSY NEEDLE
FDA Adverse Event
Malfunction
·COOK INC·Product code KNW·July 16, 2019
OSTEO-SITE BONE BIOPSY NEEDLE
FDA Adverse Event
Malfunction
·COOK INC·Product code KNW·October 8, 2019
OSTEO-SITE BONE BIOPSY NEEDLE
FDA Adverse Event
Malfunction
·COOK INC·Product code KNW·July 17, 2019
OSTEO-SITE BONE BIOPSY NEEDLE
FDA Adverse Event
Malfunction
·COOK INC·Product code KNW·July 11, 2019