631 results · 21ms · Sources: EU EUDAMED, 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