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21,387 catalysts · 4,728 grant · 3,706 8k filing · 3,504 device 510k · 2,901 approval · 2,000 device pma · 2,000 device recall
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21,387 catalysts · 4,728 grant · 3,706 8k filing · 3,504 device 510k · 2,901 approval · 2,000 device pma · 2,000 device recall
Infusion or Flow Problem
Infusion or Flow Problem
Infusion or Flow Problem
Infusion or Flow Problem
Patient Device Interaction Problem
Detachment of Device or Device Component
Infusion or Flow Problem
Leak/Splash; Material Split, Cut or Torn
Adverse Event Without Identified Device or Use Problem
Premature Discharge of Battery; Pumping Stopped
Failure to Obtain Sample
Difficult to Remove; Material Twisted/Bent
Mechanical Jam; Activation Problem
Adverse Event Without Identified Device or Use Problem
Device Dislodged or Dislocated
Insufficient Information
Therapeutic or Diagnostic Output Failure
Insufficient Information
Adverse Event Without Identified Device or Use Problem
Material Rupture
Failure to Osseointegrate
Appropriate Term/Code Not Available
Adverse Event Without Identified Device or Use Problem
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Incorrect Interpretation of Signal
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Adverse Event Without Identified Device or Use Problem
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Failure to Osseointegrate
Appropriate Term/Code Not Available
Adverse Event Without Identified Device or Use Problem