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

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    ECG ELECTRODE (VARIOUS)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295253679·INFERIOR JAW STANDARD

    CD 3700 SL

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·May 23, 2007

    B & L OPHTHALMIC CHAIR

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    e-Throne Folding Wheelchair, Model: ET-12F22

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    ACCESSORIES

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code DQX·March 20, 2025

    CELL-DYN 3700 SL ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·February 22, 2019

    PROMUS ELEMENT PLUS EVEROLIMUS-ELUTING PLATINUM CHROMIUM CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·March 6, 2013

    THE WEB EXTRACTION BASKET

    FDA Adverse Event
    Injury ·WILSON-COOK MEDICAL INC·Product code FFL·February 11, 2011

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC MILACA, INC.·Product code LWP·August 8, 2014

    ACIST

    FDA Adverse Event
    Malfunction ·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·April 20, 2007

    INDEFLATOR

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code MAV·February 27, 2024

    INDEFLATOR

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code MAV·March 21, 2024