BEUDAMED
    9 results · 22ms · Sources: EU EUDAMED, US FDA

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    PeraMobile and PeraWatch

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Shoulder Immobilizer

    FDA UDI
    MEDICAL SPECIALTIES INCORPORATED·00802357833702·

    MobileLink Acetabular Cup System

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575177165·E-Dur® Insert, shouldered 5 mm

    D-CLOT THROMBECTOMY CATHETER SYSTEM, MODEL: DC 4006

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RT200

    FDA 510(k)
    FDA Class 2 ·Neurology

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 18, 2014

    MYNXGRIP VASCULAR CLOSURE DEVICE 6F/7F

    FDA Adverse Event
    Injury ·ACCESSCLOSURE, INC.·Product code MGB·June 21, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 28, 2011

    XP-XP Tibial Tray - Interlok 63 mm Item # 195751

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·September 18, 2019