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

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    AGE AUTOMATIC UPPER ARM BLOOD PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Klaxon

    FDA UDI
    KI MOBILITY, LLC·00840363369082·Battery powered power add-on designed to provid...

    30 G X 1/2 IN. BD¿ BULK, NON-STERILE NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMF·July 27, 2017

    THE HEDROCEL TRABECULAR METAL RECONSTRUCTION SYSTEM

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

    SITE RITE PREVUE ULTRASOUND SYSTEM AND PINPOINT NEEDLE GUIDE

    FDA 510(k)
    FDA Class 2 ·Radiology

    BD VACUTAINER® SODIUM FLUORIDE BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·May 7, 2018

    PROSOUND F75 ULTRASOUND SCANNER

    FDA Adverse Event
    Malfunction ·HITACHI ALOKA MEDICAL, LTD·Product code GXX·July 16, 2014

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTN·May 22, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 27, 2014

    PROSTAR XL SUTURE-MEDIATED CLOSURE

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·June 14, 2011