52 results · 26ms · Sources: EU EUDAMED, US FDA

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ENCISION DISPOSABLE AEM CORD

FDA Adverse Event
Other ·ENCISION, INC·Product code GEI·August 10, 2004

5MM AEM HANDLE ASSEMBLY

FDA Adverse Event
Other ·ENCISION, INC.·Product code GEI·March 15, 2005

REM POLYHESIVE II

FDA Adverse Event
Other ·VALLEYLAB, INC.·Product code GEI·August 30, 1994

REM POLYHESIVE II

FDA Adverse Event
Other ·VALLEYLAB, INC.·Product code GEI·June 30, 1994

REM POLYHESIVE II

FDA Adverse Event
Other ·VALLEYLAB, INC.·Product code GEI·February 25, 1999

IV CATHETER

FDA Adverse Event
Other ·UNKNOWN·Product code LJS·June 5, 2024

ELECTRODE REM PLYHESIVE ADULT GROUNDING PAD

FDA Adverse Event
Other ·COVIDIEN·Product code GEI·May 24, 2024

WECK IMAENT BLADE

FDA Adverse Event
Other ·WECK PILLING WECK·Product code GEI·September 13, 2001

ELECTRODE REM PLYHESIVE ADULT GROUNDING PAD

FDA Adverse Event
Other ·COVIDIEN·Product code GEI·May 24, 2024

ELECTRODE REM PLYHESIVE ADULT GROUNDING PAD

FDA Adverse Event
Other ·COVIDIEN·Product code GEI·May 24, 2024

ELECTRODE REM PLYHESIVE ADULT GROUNDING PAD

FDA Adverse Event
Other ·COVIDIEN·Product code GEI·May 24, 2024

VALLEYLAB REM POLYHESIVE II

FDA Adverse Event
Other ·TYCO HEALTHCARE GROUP LP·Product code GEI·November 29, 2004

VULCAN GENERATOR

FDA Adverse Event
Other ·SMITH & NEPHEW, INC.- ENDOSCOPY DIV·Product code HRX·June 6, 2006

NEONATAL REM POLYHESIVE II

FDA Adverse Event
Other ·VALLEYLAB, DIV OF TYCO HEALTHCARE GROUP LP·Product code GEI·September 30, 2003

VALLEY LAB REM POLYHESIVE

FDA Adverse Event
Other ·VALLEY LAB·Product code JOS·September 8, 2004

WHEELCHAIR, BARIATRIC, 28", REM

FDA Adverse Event
Other ·MEDLINE INDUSTRIES, INC.·Product code IOR·March 4, 2008

REM POLY HESIVE II

FDA Adverse Event
Other ·VALLEY LAB, INC.·Product code GEI·February 10, 1999

REM POLY HESIVE II

FDA Adverse Event
Other ·VALLEY LAB, INC.·Product code GEI·February 25, 1999

WHEELCHAIR,BARIATRIC,26",REM F

FDA Adverse Event
Other ·MEDLINE INDUSTRIES, INC.·Product code IOR·May 25, 2010

WHEELCHAIR, BARIATRIC, 28", REM D

FDA Adverse Event
Other ·MEDLINE INDUSTRIES, INC.·Product code IOR·June 19, 2007