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

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    AESCULAP MODULAR MONOPOLAR ELECTRODES

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CERAMIC ELECTRODE TIP L-HK F/GK372R

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code GEI·July 5, 2019

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970541·anteriors; shade BL3; mould UCL

    Anorganic Bone Mineral in Delivery Applicator

    FDA 510(k)
    FDA Class 2 ·Dental

    IVIVI SOFPULSE, MODELS 912-M10, ROMA3 AND TORINO II

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    SEE H10

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code NBC·April 18, 2013

    VERITAS COLLAGEN MATRIX

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code FTM·February 20, 2013

    INTEGRATED APD SET W/CASSETTE3-PRONG

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·January 25, 2011

    M2A-MAGNUM MOD HD SZ 52MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 31, 2014