1,555 results · 25ms · Sources: EU EUDAMED, US FDA

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SHOCKPULSE LITHOTRIPSY TRANSDUCER.

FDA Adverse Event
Malfunction ·GYRUS ACMI INC·Product code FEO·August 18, 2020

SHOCKPULSE-SE LITHOTRIPSY SYSTEM (REUSAB

FDA Adverse Event
Malfunction ·GYRUS ACMI INC·Product code FEO·August 12, 2020

SHOCKPULSE-SE LITHOTRIPSY SYSTEM

FDA Adverse Event
Malfunction ·GYRUS ACMI INC·Product code FEO·September 17, 2020

SHOCKPULSE-SE LITHOTRIPSY SYSTEM

FDA Adverse Event
Malfunction ·GYRUS ACMI INC·Product code FEO·August 5, 2020

SHOCKPULSE-SE LITHOTRIPSY SYSTEM

FDA Adverse Event
Malfunction ·GYRUS ACMI INC·Product code FEO·July 20, 2020

SHOCKPULSE LITHOTRIPSY PROBE, REUSABLE,

FDA Adverse Event
Malfunction ·GYRUS ACMI INC·Product code FEO·September 11, 2020

SHOCKPULSE LITHOTRIPSY TRANSDUCER.

FDA Adverse Event
Malfunction ·GYRUS ACMI INC·Product code FEO·August 31, 2020

SHOCKPULSE LITHOTRIPSY TRANSDUCER.

FDA Adverse Event
Malfunction ·GYRUS ACMI INC·Product code FEO·August 20, 2020

SHOCKPULSE LITHOTRIPSY PROBE, REUSABLE,

FDA Adverse Event
Malfunction ·GYRUS ACMI INC·Product code FEO·September 8, 2020

SHOCKPULSE LITHOTRIPSY TRANSDUCER.

FDA Adverse Event
Malfunction ·GYRUS ACMI INC·Product code FEO·August 7, 2020

SHOCKPULSE-SE LITHOTRIPSY SYSTEM

FDA Adverse Event
Malfunction ·GYRUS ACMI INC·Product code FEO·September 25, 2020

SHOCKPULSE LITHOTRIPSY TRANSDUCER.

FDA Adverse Event
Malfunction ·GYRUS ACMI INC·Product code FEO·July 6, 2020

SHOCKPULSE-SE LITHOTRIPSY SYSTEM

FDA Adverse Event
Malfunction ·GYRUS ACMI INC·Product code FEO·September 21, 2020

SHOCKPULSE-SE LITHOTRIPSY SYSTEM (REUSAB

FDA Adverse Event
Malfunction ·GYRUS ACMI INC·Product code FEO·August 27, 2020

SHOCKPULSE PROBE SINGLE USE, 3.76MM 3/BX

FDA Adverse Event
Malfunction ·GYRUS ACMI INC·Product code FEO·August 17, 2020

SHOCKPULSE PROBE SINGLE USE, 3.40MM 3/BX

FDA Adverse Event
Malfunction ·GYRUS ACMI INC·Product code FEO·July 23, 2020

SHOCKPULSE-SE LITHOTRIPSY SYSTEM

FDA Adverse Event
Malfunction ·GYRUS ACMI INC·Product code FEO·September 14, 2020

SHOCKPULSE LITHOTRIPSY TRANSDUCER.

FDA Adverse Event
Malfunction ·GYRUS ACMI INC·Product code FEO·August 10, 2020

SHOCKPULSE LITHOTRIPSY TRANSDUCER.

FDA Adverse Event
Malfunction ·GYRUS ACMI INC·Product code FEO·July 8, 2020

SHOCKPULSE LITHOTRIPSY TRANSDUCER.

FDA Adverse Event
Malfunction ·GYRUS ACMI INC·Product code FEO·July 16, 2020