BEUDAMED
    6 results · 19ms · 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 Regulation: Us FDA ×

    MODULAR REACH HIP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COMPACT TOUCH

    FDA 510(k)
    FDA Class 2 ·Radiology

    PLUME-AWAY SMOKE EVACUATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    UNKNOWN DEPUY BONE SCREW

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code HWC·March 8, 2013

    CELL-DYN 1800 ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·February 16, 2011

    HUDSON PEDIATRIC BREATHING CIRCUIT, 30"

    FDA Adverse Event
    Malfunction ·TELEFLEX·Product code OFP·July 24, 2014