BEUDAMED
    9 results · 24ms · Sources: EU EUDAMED, US FDA

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    DePuy Synthes Craniomaxillofacial Sternal Devices - MR Conditional

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR, MODEL KD-556

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 2, 2024

    HEARTMATE 3 VAD MODULAR CABLE

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·August 18, 2023

    ECHELON MICRO CATHETER

    FDA Adverse Event
    Injury ·EV3 NEUROVASCULAR·Product code KRA·August 4, 2011

    MATOME STEREOTACTIC 11 G PROBE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code KNW·October 9, 2008

    6000CMS

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·June 14, 2013

    THORATEC® HEARTMATE 3¿ VAD MODULAR CABLE

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·February 5, 2024