631 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ENDURANT STENT GRAFT
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code MIH·July 23, 2018
ENDURANT STENT GRAFT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·July 23, 2018
IVENIX INFUSION SYSTEM
FDA Adverse Event
Malfunction
·FRESENIUS KABI USA LLC·Product code FRN·August 26, 2024
MYOMA SCREW
FDA Adverse Event
Injury
·JARIT/INTEGRA·Product code HHO·June 24, 2010
MYOMA SCREW
FDA Adverse Event
Malfunction
·RICHARD WOLF MEDICAL INSTRUMENTS CORP.·Product code HHO·August 21, 1997
CASPAR CERVICAL SCREW
FDA Adverse Event
Malfunction
·UNKNOWN·Product code HHO·May 20, 1995
MYOMA SCREWS
FDA Adverse Event
Injury
·INTEGRA-JARET INSTRUMENTS·Product code HHO·December 11, 2012
UTERINE CORKSCREW
FDA Adverse Event
Malfunction
·WISAP·Product code HHO·May 9, 1994
ENDURANT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·May 14, 2015
REZUM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·April 21, 2026
PLATE,FIXATION,BONE
FDA Adverse Event
Injury
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·April 23, 2018
PLATE,FIXATION,BONE
FDA Adverse Event
Injury
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·April 23, 2018
SCREW,FIXATION,BONE
FDA Adverse Event
Injury
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·April 23, 2018
SCREW,FIXATION,BONE
FDA Adverse Event
Injury
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·April 23, 2018
Screw, Fibroid, Gynecological
FDA classification
FDA Class 2
·Screw, Fibroid, Gynecological
mixsoon Derma Booster PRO
FDA UDI
Haho Medi·08809732914683·personal home care facial massage device
HindexRV
FDA UDI
HHS SYSTEMS, INC.·00860001651911·The HindexRV® Monitoring System is a physiologi...
HindexRV
FDA UDI
HHS SYSTEMS, INC.·00860001651904·The HindexRV® Monitoring System is a physiologi...
HAHO MEDI
FDA registration
HAHO MEDI·1 product·🇰🇷 South Korea
CPCS COCR PRIM HO 12/14 SZ 2
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code JDI·May 5, 2018