6 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
COHEN INTRAUTERINE PROBE
FDA Adverse Event
Malfunction
·TROKAMED GMBH·Product code ---·January 4, 2006
GRIP MODUL V2.0, 5-TIMES-USE MORCELLATOR SYSTEM
FDA Adverse Event
Malfunction
·TROKAMED GMBH·Product code HET·June 27, 2023
MYOMA SCREW 5MM, 32CM
FDA Adverse Event
Malfunction
·TROKAMED GMBH·Product code MDM·July 17, 2007
ADAPTER FOR COHEN CANNULA
FDA Adverse Event
Malfunction
·TROKAMED GMBH·Product code GCJ·June 7, 2016
GRIP MODUL V2.0, 5-TIMES-USE MORCELLATOR SYSTEM
FDA Adverse Event
Malfunction
·TROKAMED GMBH·Product code HET·December 5, 2023
MYOMA SCREW 5MM, 32CM
FDA Adverse Event
Malfunction
·TROKAMED HENGSTLER GMBH·Product code KOG·December 5, 2003