435 results
·
56ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
×
ERBE USA INC.
FDA Adverse Event
Injury
·ERBE USA INC·Product code GEI·March 11, 2002
ERBE USA, INC.
FDA Adverse Event
Injury
·ERBE USA, INC.·Product code GEI·March 21, 2006
ERBE USA, INC.
FDA Adverse Event
Injury
·ERBE USA INC.·Product code GEI·May 16, 1998
ERBE USA INC.
FDA Adverse Event
Injury
·ERBE USA INC.·Product code GEI·November 6, 2015
ERBE APC 300
FDA Adverse Event
Injury
·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·December 11, 2006
UNKNOWN
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·August 10, 2022
ERBOTOM ICC 200 E
FDA Adverse Event
Injury
·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·April 30, 2008
ERBE VIO 300 D
FDA Adverse Event
Injury
·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·September 19, 2016
ERBE BICLAMP LAPAROSCOPIC INSTRUMENTS
FDA Adverse Event
Injury
·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·April 14, 2017
UNKNOWN
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·August 24, 2022
ERBOTOM ICC 350
FDA Adverse Event
Injury
·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·December 7, 2021
ERBE VIO DV
FDA Adverse Event
Injury
·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·March 11, 2025
ERBE BICLAMP LAPAROSCOPIC INSTRUMENTS
FDA Adverse Event
Injury
·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·December 16, 2016
ERBE VIO 200 D
FDA Adverse Event
Injury
·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·July 15, 2016
ERBE APC 2
FDA Adverse Event
Injury
·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·April 14, 2022
ERBE APC 2
FDA Adverse Event
Injury
·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·August 16, 2022
ERBE APC 2
FDA Adverse Event
Injury
·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·January 9, 2009
ERBE VIO 300 D
FDA Adverse Event
Injury
·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·May 21, 2020
ERBE VIO 300 D
FDA Adverse Event
Injury
·ERBE ELECTROMEDIZIN GMBH·Product code GEI·September 23, 2009
ERBE APC 300
FDA Adverse Event
Injury
·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·October 18, 2022