52 results
·
26ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Other
×
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