BEUDAMED
    8 results · 26ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    862451

    FDA Adverse Event
    Death ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code DSI·February 20, 2026

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BASTER HEALTHCARE CORPORATION·Product code FRN·January 23, 2014

    2520274-2012-03659

    FDA Adverse Event
    Injury ·SYNTHES·Product code JDI·December 10, 2012

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·June 23, 2015

    11MM/130 DEG TI CANN TROCH IXATION NAIL 400MM/RIGHT-STER

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HSB·May 18, 2015

    11.0MM TI HELICAL BLADE 95MM-STERILE

    FDA Adverse Event
    Malfunction ·SYNTHES ELMIRA·Product code HSB·May 18, 2015

    PERCUTANEOUS CANN CONNECTING SCREW F/TROCH FIXATION NAILS

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code LXH·May 15, 2015

    BLADE GUIDE SLEEVE FOR TROCHANTERIC FIXATION NAILS

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code FZX·May 15, 2015