40 results
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28ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Canon OCT-A1
FDA 510(k)
FDA Class 2
·Ophthalmic
MODFICATION TO: EXPEDIUM SPINE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
CORELEADER ALGIPLASTER MODEL AP 050501
FDA 510(k)
FDA Unclassified
·Unknown
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
NIPRO BLOOD TUBING SET W/TP
FDA Adverse Event
Malfunction
·NIPRO (THAILAND) CORP. LTD.·Product code FJK·February 6, 2024
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 6, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 4, 2021
SURDIAL X
FDA Adverse Event
Malfunction
·SHIBUYA (SBY)·Product code KDI·August 5, 2021
NIPRO BLOOD TUBING SET W/TP
FDA Adverse Event
Injury
·NIPRO (THAILAND) CORP. LTD.·Product code FJK·January 17, 2024