BEUDAMED
    7 results · 27ms · Sources: EU EUDAMED, US FDA

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    HEWLETT-PACKARD MODEL M1490A WIRELESS PATIENT DATA COMMUNICATOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MICRO-AIRE 4220-000 OSCILLATING SAW

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    ENDOTRACHEAL CPAP SET

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    HEARTSTART XL - DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 6, 2014

    TAPERED U-JOINT DRIVER FOR SYNFIX MINI-OPEN

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code MAX·February 1, 2013

    UNKNOWN SIZE 58 DEPUY SROM CUP

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·December 30, 2010

    EVOLUT FX DCS

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NPT·September 8, 2025