BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    KELSEY INTERSITITAL LASER THERAPY SYSTEM

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

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306814457·Gemini Forceps, (Mixter), Angled, 30.5 cm

    OMNIA X/XS ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    MED-LOGICS DISPOSABLE ALK TUBING

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    ASR TAP SLV ADAP 12/14 -1

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD.·Product code KWA·March 17, 2016

    ON-Q C-BLOC: 400 ML, 2-14 ML/HR SAF + 5 ML/30MIN

    FDA Adverse Event
    Malfunction ·I-FLOW, LLC·Product code MEB·April 17, 2013

    LIFEPAK CR PLUS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·June 30, 2008

    BASIC CONFIGURATION MODEL 6100 BASE

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·April 18, 2011

    VITROS IMMUNODIAGNOSTIC PRODUCTS TSH REAGENT PACK

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code JLW·February 2, 2016

    VITROS ECI IMMUNODIAGNOSTIC SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KHO·February 2, 2016