BEUDAMED
    13 results · 23ms · Sources: EU EUDAMED, US FDA

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    INTRALASE FS LASER, INTRALASE FS30 LASER, MODELS 1, 2, 3

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

    INTRALASE FS2

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HNO·November 21, 2013

    VISX EXCIMER LASER

    FDA Adverse Event
    Injury ·AMO MANUFACTURING USA LLC·Product code LZS·November 5, 2010

    INTRALASE FS2

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HNO·August 20, 2013

    INTRALASE FS2

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HNO·October 30, 2013

    REMEL

    FDA UDI
    REMEL, INC.·00848838006234·Campy Thio Medium w/Agar (9ml) 20/PK

    LIGHTLAS 532 PHOTOCOAGULATOR

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    MODIFICATION TO EBI DYNAFIX DIAPHYSEAL CORRECTION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYR 10ML PUMP COMPATIBLE SALINE 10ML FIL

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·January 24, 2020

    BD¿ SYR 10ML PUMP COMPATIBLE SALINE 10ML FIL

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·January 27, 2020

    8800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 10, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Injury ·LIFESCAN INC.·Product code NBW·April 15, 2011

    CENTRAX DURATION 26MM X 51MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JDI·June 11, 2008