BEUDAMED
    9 results · 27ms · Sources: EU EUDAMED, US FDA

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    APOLLO REVISION/CONSTRAINED KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SpineWand

    FDA UDI
    MORGAN STEER ORTHOPAEDICS LIMITED·05060696460019·Perc DLG Convenience Pack inc 17 gauge 8” Crawf...

    Coblation

    FDA UDI
    Smith & Nephew, Inc.·00817470004489·PERC DLG

    iNSitu Total Hip System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PLS MINI

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MARYLAND BIPOLAR FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·February 21, 2013

    MX-PRO R-3 AMBULANCE COT

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIV.·Product code INK·December 30, 2010

    OT VERIO TEST STRIPS

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 1, 2014

    JTS External Drive Unit JTS Distal Femoral Extendible Implant Femur is intended for the replacement of diseased or deficient bone in the distal femur.

    FDA Recall
    Terminated ·Stanmore Implants Worldwide Ltd. Centennial Park·Product code KRO·July 4, 2017