7 results
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23ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
SURESTEP
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CGA·August 20, 1999
ANGEL SYSTEM WITH ASPIRATION KIT W/ ACDA
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code ORG·March 5, 2019
ARTHREX ANGEL SYSTEM WITH ASPIRATION KIT
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code ORG·May 1, 2019
CONSTELLATION VISION SYSTEM
FDA Adverse Event
Injury
·ALCON-IRVINE TECHNOLOGY CENTER·Product code HQC·May 23, 2013
SPRINT QUATTRO SECURE
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·June 16, 2011
MBT CEM KEEL TIB TRAY SZ2.5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, DEPUY CORK DIVISION·Product code NJL·August 20, 2008
MITRACLIP G4 CLIP DELIVERY SYSTEM (MDD)
FDA Adverse Event
Malfunction
·ABBOTT MEDICAL·Product code NKM·March 7, 2024