BEUDAMED
    12 results · 24ms · Sources: EU EUDAMED, US FDA

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    NEEDLEGARD II

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110928·STERILIZING CASE SINGLE VR

    Accu-Beam

    FDA UDI
    TRANSAMERICAN TECHNOLOGIES INTERNATIONAL·B1779207170·Re-usable fiberoptic handpiece for lasers. 17ga...

    SYNTHES VARIABLE ANGLE LCP ELBOW SYSTEM (MEDICAL AND POSTEROLATERAL DISTAL HUMERUS PLATES)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EBV V VCA IGM ELISA KIT MODEL# EBM-200

    FDA 510(k)
    FDA Class 1 ·Microbiology

    PREMISE PACKABLE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·July 11, 2014

    PREMISE PACKABLE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·July 11, 2014

    PREMISE PACKABLE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·July 11, 2014

    PREMISE PACKABLE

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·July 11, 2014

    TALENT CAPTIVIA THORACIC STENT GRAFT SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code MIH·December 9, 2010

    ASR ACETABULAR IMPLANT 50

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 17, 2013

    VERITY ADX XL

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWP·July 8, 2014