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

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    ZVPLASTY

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    3M™ Unitek™

    FDA UDI
    3M UNITEK CORPORATION·00652221037442·Unitek(TM) Bicuspid Band General Purpose Wide L...

    K2M General Instruments

    FDA UDI
    VB Spine LLC·10888857581142·Split Tube Retractor Ø14x110 mm

    ENSITE VELOCITY SYSTEM, MODEL EE3000

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LIGHTFORCE LF 20/30 980NM SURGICAL DIODE LASER SYSTEM

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

    VERCISE? CARTESIA?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code PJS·February 17, 2026

    OT VERIO SYNC METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 4, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013

    SM304 M-SERIES W/ZOOM

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·June 1, 2011

    GMK-SPHERE FEMORAL COMPONENT CEMENTED SIZE 4 LEFT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·February 8, 2017