BEUDAMED
    10 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Reprocessed AcuNav Diagnostic Ultrasound Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SHASER IPL HAIR REMOVAL SYSTEM

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

    HILGER DUAL-STIM NERVE STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·June 11, 2013

    FIXODENT DENTURE ADHESIVE, ORIGINAL (CALCIUM ZINC GANTREZ SALT 33%, CELLULOSE GU

    FDA Adverse Event
    Other ·PROCTER & GAMBLE MANUFACTURING CO.·Product code KOO·June 2, 2011

    APEX MONORAIL

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code LOX·September 17, 2008

    TRUFILL DCS ORBIT DETACHABLE COIL SYSTEM

    FDA Adverse Event
    Malfunction ·CODMAN AND SHURTLEFF, INC·Product code HCG·June 15, 2017

    M2A MAGNUM 42-50M TPR INSRT +6

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·May 23, 2018

    M2A-MAGNUM MOD HD SZ 46MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·May 23, 2018

    BI-METRIC/X POR NC 11X135

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·May 23, 2018