BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    XENON LIGHT SOURCE AUTO LIP 5123, MODEL 2123.011

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    STERLING

    FDA UDI
    BENCO DENTAL SUPPLY CO.·00366975003652·Sterling Diode Laser Replacement Handpiece

    Arthrex TensionLoc System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GLUCODR AUTO SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    COULTER® LH 750 HEMATOLOGY ANALYXZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·February 28, 2013

    UNKNOWN DEPUY 58MM HYLAMER LINER

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·January 31, 2011

    STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LGW·August 6, 2014

    BIOMET MICROFIXATION MANDIBULAR FRACTURE/ RECONSTRUCTION DEVICES

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HWC·June 3, 2016