23 results · 22ms · Sources: EU EUDAMED, US FDA

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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