BEUDAMED
    460 results · 27ms · Sources: EU EUDAMED, US FDA

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    Disposable Nitrile Gloves

    FDA 510(k)
    FDA Class 1 ·General Hospital

    EVOS Lumbar Interbody System

    FDA UDI
    Cutting Edge Spine, LLC·00841193100623·EVOS Straight HA PEEK, 9mm x 8mm x 22mm, Flat 5...

    PROFYLE

    FDA UDI
    Stryker GmbH·07613153169086·1.2mm Outer Sheath

    MEGA5.5 SPINE SYSTEM

    FDA UDI
    BK MEDITECH CO.,LTD.·08809228125654·Rod, Ø5.5 x 90mm

    DVX5.5 SPINE SYSTEM

    FDA UDI
    BK MEDITECH CO.,LTD.·08809228126538·Rod, Ø5.5 x 90mm

    MX8000 IDT CT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    AIDA VI.8 DIAGNOSTIC ULTRASOUND GM-72P00A, L13-5V1 TRANSDUCER

    FDA 510(k)
    FDA Class 2 ·Radiology

    ETS-FLEX - ENDOSCOPIC ARTICULATING LINEAR CUTTER (VASCULAR/THIN) - 35MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC·Product code GDW·September 21, 2009

    LUMAX 340 DR-T

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code LWS·December 23, 2009

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code MCM·August 28, 2009

    ACCU-CHEK MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·April 24, 2009

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 29, 2014

    PROMUS ELEMENT ¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·August 15, 2011

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·July 8, 2013

    LADARVISION 4000 LASER

    FDA Adverse Event
    Injury ·ALCON- ORLANDO TECHNOLOGY CENTER·Product code LZS·August 21, 2009

    TRUWAVE DISPOSABLE PRESSURE TRANSDUCER

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code DRS·February 13, 2009

    M230 SENSI-TCH 22X4-1/2

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code BSP·January 22, 2008

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD·Product code MCM·April 21, 2009

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSTEMS·Product code LZG·August 20, 2009

    16FR SILVER DRAIN BAG FOLEY TR

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code KOD·April 22, 2009