BEUDAMED
    12 results · 20ms · Sources: EU EUDAMED, US FDA

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    MODIFICATION TO: HI-ART SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    Mini-Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR70609121·Mini Sprint-Brackets Roth .018" 100 Brackets

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07311K0600120·Tray Insert 5, Cosmolock Deformity

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07310K0690120·Tray Insert, MIS Lumbar Instruments 1

    ALARMVIEW WIRELESS DATA NETWORK SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SIMPLICITY EASY SOFT INFUSION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BIOLOX PROSTHESIS HEAD 12/14 28MM S

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code LWJ·April 14, 2014

    BIOLOX PROSTHESIS HEAD 12/14 28MM S

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code LWJ·March 6, 2014

    ASR ACETABULAR IMPLANT 52

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·April 16, 2013

    NOVA MAX GLUCOSE MONITOR

    FDA Adverse Event
    Malfunction ·NOVA BIOMEDICAL CORPORATION·Product code NBW·March 14, 2011

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code IOR·September 4, 2014

    X3 TRIATHLON CS INSERT #5 9MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·July 1, 2013