BEUDAMED
    7 results · 30ms · Sources: EU EUDAMED, US FDA

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    EXHALATION VALVE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Polystar HK

    FDA UDI
    Merz Dental GmbH·D7091984481·anteriors; shade C2; mould 91

    INSUFFLATION TUBING

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    CLEAR SHOT ANGIOPLASTY BALLOON INFLATION DEVICE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·February 28, 2013

    ASR ACETABULAR CUPS 58

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·January 27, 2011

    LINOX SMART S DX 65/17

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVY·August 6, 2014