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