576 results
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34ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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SBI PIP IMPLANT
FDA Adverse Event
Other
·SBI·Product code MPK·April 13, 2007
SBI - SMALL BONE INNOVATIONS
FDA Adverse Event
Injury
·SBI·Product code KWI·April 1, 2008
CARDIOSAVE
FDA Adverse Event
Malfunction
·DATASCOPE MAHWAH·Product code DSP·January 10, 2019
PRIDE MOBILITY PRODUCTS
FDA Adverse Event
Injury
·PRIDE MOBILITY PRODUCTS·Product code ITI·June 9, 2023
AMBULIFT BSQ
FDA Adverse Event
Other
·ARJO LTD.·Product code FSA·July 26, 2000
AMBULIFT BSQ
FDA Adverse Event
Malfunction
·ARJO LTD.·Product code FSA·October 30, 2001
AMBULIFT BSQ
FDA Adverse Event
Malfunction
·ARJO LTD.·Product code FSA·November 19, 2001
AMBULIFT BSQ
FDA Adverse Event
Malfunction
·ARJO, LTD.·Product code FSA·September 21, 2001
AMBULIFT BSQ
FDA Adverse Event
Malfunction
·ARJO HOSPITAL EQUIPMENT AB·Product code FSA·July 22, 2010
SURDIAL DX HEMODIALYSIS SYSTEM AND ACCESSORIES
FDA Adverse Event
Death
·SHIBUYA (SBY)·Product code KDI·May 23, 2022
SURDIAL DX HEMODIALYSIS SYSTEM AND ACCESSORIES
FDA Adverse Event
Injury
·SHIBUYA (SBY)·Product code KDI·May 23, 2022
NIPRO SURDIAL DX HEMODIALYSIS SYSTEM
FDA Adverse Event
Death
·SHIBUYA (SBY)·Product code KDI·August 1, 2024
NIPRO SURDIAL DX HEMODIALYSIS SYSTEM
FDA Adverse Event
Death
·SHIBUYA (SBY)·Product code KDI·August 1, 2024
SURDIAL DX HEMODIALYSIS SYSTEM AND ACCESSORIES
FDA Adverse Event
Death
·SHIBUYA (SBY)·Product code KDI·May 23, 2022
NIPRO SURDIAL DX HEMODIALYSIS SYSTEM
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·May 4, 2026
NIPRO SURDIAL DX HEMODIALYSIS SYSTEM
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·April 27, 2026
NIPRO SURDIAL DX HEMODIALYSIS SYSTEM
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·April 27, 2026
NIPRO SURDIAL DX HEMODIALYSIS SYSTEM
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·April 27, 2026
NIPRO SURDIAL DX HEMODIALYSIS SYSTEM
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·September 24, 2025
NIPRO SURDIAL DX HEMODIALYSIS SYSTEM
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·September 25, 2025