BEUDAMED
    176 results · 24ms · Sources: EU EUDAMED, US FDA

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    Bausch + Lomb PreVue Inserter for enVista Preloaded

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    PureLife+ Sterilization Pouches

    FDA UDI
    PURELIFE, LLC·D79011920051·PureLife+ Sterilization Pouches, 5 1/4" x 10", ...

    Bernafon

    FDA UDI
    Bernafon AG·05711584086797·ZR3, KIT 312 2.4G NFM PB L BE ZERENA 3

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776199814·LLETZ GRAVES SPEC LRG wEVAC

    ALLURA XPER OR TABLE SERIES

    FDA 510(k)
    FDA Class 2 ·Radiology

    NON-STERILE, POWDER-FREE, GREEN LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LESS)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    DORNIER HOLMIUM LASER FIBER

    FDA Adverse Event
    Malfunction ·DORNIER MEDTECH AMERICA, INC.·Product code GEX·July 13, 2007

    BIOGLUE SURGICAL ADHESIVE

    FDA Adverse Event
    Malfunction ·CRYOLIFE, INC.·Product code MFI·September 19, 2006

    INFINITY VISION SYSTEM

    FDA Adverse Event
    Injury ·ALCON-IRVINE TECHNOLOGY CENTER·Product code HQE·April 7, 2005

    EASY PUMP

    FDA Adverse Event
    Other ·I-FLOW CORP.·Product code MEB·March 30, 2006

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·November 22, 2005

    BIOBLUE SURGICAL ADHESIVE

    FDA Adverse Event
    Injury ·CRYOLIFE, INC.·Product code MFI·September 19, 2006

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code LWS·February 9, 2006

    THUMPER

    FDA Adverse Event
    Malfunction ·MICHIGAN INSTRUMENTS·Product code DRM·October 20, 2005

    VITALITY DS

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code LWS·August 9, 2006

    CLARION

    FDA Adverse Event
    Malfunction ·ADVANCED BIONICS CORPORATION·Product code MCM·October 13, 2005

    ALARIS SYRINGE MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 2, 2020

    SYNCHROMED EL

    FDA Adverse Event
    Injury ·RICE CREEK MANUFACTURING·Product code LKK·November 23, 2005

    ORTHO PROVUE ANALYZER

    FDA Adverse Event
    Malfunction ·MICRO TYPING SYSTEMS, INC.·Product code KSZ·November 17, 2005

    UNK ELECTROSURGICAL PENCIL

    FDA Adverse Event
    Malfunction ·VALLEYLAB·Product code GEI·April 5, 2006