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

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    CAMERA ENABLED PROBE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EXPEDIUM SPINE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYNGO DOSIMETRIST WORKSPACE V2.7 MODEL: 1056864

    FDA 510(k)
    FDA Class 2 ·Radiology

    Widex

    FDA UDI
    Widex A/S·05706069920369·WIDEX MOMENT MBB3D 440 DEMO (Silver grey)

    Widex

    FDA UDI
    Widex A/S·05706069884791·WIDEX MOMENT MRR2D DEMO (Silver Grey ) 440, RC ...

    Widex

    FDA UDI
    Widex A/S·05706069886627·WIDEX MOMENT MRB0 (Silver Grey ) 440, RIC 10

    Widex

    FDA UDI
    Widex A/S·05706069812619·Widex EVOKE E-PA (Silver Grey ) 440, RC coil

    23 G X 1 IN. BD ECLIPSE¿ HYPODERMIC NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FMI·November 23, 2016

    MYAIRVO HUMIDIFIER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·July 16, 2015

    SYNGO SUITE FOR ONCOLOGY SYSTEM

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SOLUTIONS USA, INC.·Product code MUJ·November 9, 2012

    ASR ACETABULAR CUPS 58

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·June 3, 2013

    VISIAN ICL (IMPLANTABLE COLLAMER LENS)

    FDA Adverse Event
    Injury ·STAAR SURGICAL COMPANY·Product code MTA·June 22, 2011

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·October 3, 2014

    AIRVO2 HUMIDIFIER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·December 1, 2015