10,000 results · 25ms · Sources: EU EUDAMED, US FDA

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UNKNOWN CUSA EXCEL

FDA Adverse Event
Injury ·INTEGRA LIFESCIENCES(IRELAND)·Product code LFL·May 11, 2018

HARMONIC SCALPEL CURVED SHEAR (EXACT CODE UNKNOWN)

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GEI·July 1, 2025

HARMONIC ACE 5MM SHEAR

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·July 2, 2025

Hand of Hope

FDA UDI
Rehab-Robotics Company Limited·04897113220090·The Hand of Hope (HOH) is a therapy device (exo...

Hand of Hope

FDA UDI
Rehab-Robotics Company Limited·04897113220021·The Hand of Hope (HOH) is a therapy device (exo...

UNKNOWN LIGASURE INSTRUMENT

FDA Adverse Event
Injury ·COVIDIEN MFG DC BOULDER·Product code GEI·October 31, 2020

HARMONIC ACE 5MM SHEAR

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·September 28, 2020

THUNDERBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP TYPE S

FDA Adverse Event
Injury ·AOMORI OLYMPUS CO., LTD.·Product code GEI·December 30, 2024

HARMONIC ACE 5MM SHEAR

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·August 4, 2023

HARMONIC ACE 5MM SHEAR

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·August 4, 2023

HARMONIC ACE 5MM SHEAR

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·August 4, 2023

HARMONIC ACE 5MM SHEAR

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·August 4, 2023

HARMONIC ACE 5MM SHEAR

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·August 4, 2023

HARMONIC ACE 5MM SHEAR

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·August 4, 2023

HARMONIC ACE 5MM SHEAR

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·August 4, 2023

HARMONIC ACE 5MM SHEAR

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·October 18, 2024

HARMONIC ACE 5MM SHEAR

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·September 28, 2020

CYPHER SIROLIMUS-ELUTING CORONARY STENT

FDA Adverse Event
Injury ·CORDIS LLR (PR)·Product code NIQ·July 30, 2003

UNKNOWN COOL TIP ELECRTRODE

FDA Adverse Event
Malfunction ·COVIDIEN MFG DC BOULDER·Product code NEY·July 23, 2024

UNKNOWN COOL TIP ELECRTRODE

FDA Adverse Event
Injury ·COVIDIEN MFG DC BOULDER·Product code NEY·July 23, 2024