23 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·November 12, 2024
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·January 19, 2025
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·October 28, 2024
9616240-2006-00341
FDA Adverse Event
Malfunction
·Product code FII·June 14, 2006
9616240-2006-00332
FDA Adverse Event
Other
·Product code FII·June 1, 2006
PHOENIX
FDA Adverse Event
Malfunction
·GAMBRO DASCO·Product code FII·May 10, 2006
9616240-2006-00339
FDA Adverse Event
Malfunction
·Product code FII·June 9, 2006
9616240-2006-00340
FDA Adverse Event
Malfunction
·Product code FII·June 9, 2006
9616240-2006-00350
FDA Adverse Event
Malfunction
·Product code FII·June 23, 2006
9616240-2006-00345
FDA Adverse Event
Malfunction
·Product code FII·June 14, 2006
CARDIOSAVE HYBRID, TYPE I PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·February 3, 2026
PHOENIX
FDA Adverse Event
Malfunction
·GAMBRO DASCO·Product code FII·May 10, 2006
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·July 20, 2025
PHOENIX
FDA Adverse Event
Malfunction
·GAMBRO DASCO·Product code FII·May 10, 2006
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·September 17, 2025
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·December 5, 2024
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·February 25, 2025
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·December 17, 2025
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·December 8, 2024
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·February 24, 2025