BEUDAMED
    11 results · 22ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    PROBE SHEATH FOR ADMS ULTRASOUND PROBE

    FDA 510(k)
    FDA Class 2 ·Radiology

    dentaform®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011881208220·dentaform® Snap Band, Tooth 36, Size 8/Roth 22

    dentaform®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011881208180·dentaform® Snap Band, Tooth 36, Size 8/Roth 18

    dentaform®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011881208000·dentaform® Snap Band, Tooth 36, Size 8

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·November 5, 2014

    4CIS VANE SPINE SYSTEM

    FDA Adverse Event
    Injury ·SOLCO BIOMEDICAL CO., LTD·Product code MNI·December 3, 2009

    CINCH ANCHOR, MODEL 1194

    FDA 510(k)
    FDA Class 2 ·Neurology

    Vygon Midline 3 Fr SL Catheter; Vygon Midline 4 Fr SL Catheter; Vygon Midline 5 Fr DL Catheter

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ENDO CLIP LRGE 10MM PISTOL GRIP APPLIER

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL·Product code GDO·October 20, 2010

    DURATA STS OPTIM ACTIVE FIXATION LEAD, DF4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL INC., CARDIAC RHYTHM MANAGEMENT D·Product code NVY·January 13, 2014

    ASR UNI FEMORAL IMPL SIZE 49

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·December 20, 2012