4 results
·
14ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
BIOSOFT DUO DOUBLE LOOP URETERAL STENT KIT
FDA Adverse Event
Malfunction
·COLOPLAST A/S·Product code FAD·September 3, 2024
BIOSOFT DUO DOUBLE LOOP URETERAL STENT KIT
FDA Adverse Event
Malfunction
·COLOPLAST A/S·Product code FAD·December 20, 2024
SM204 M-SERIES W/BIG WHEEL
FDA Adverse Event
Malfunction
·STRYKER CORP. MEDICAL DIVISION·Product code FPO·October 13, 2010
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 16, 2012