BEUDAMED
    512 results · 23ms · Sources: EU EUDAMED, US FDA

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    ULTRASONIC TABLETOP DOPPLER; ULTRASONIC TABLETOP DOPPLER

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776350673·Stevens Tenotomy SuperCut Scissors

    THORATEC® HEARTMATE II®, SPANNER WRENCH

    FDA UDI
    Thoratec Corporation·00813024010210·

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780375234·Integra® Jarit® Stevens Tenotomy Scissors, 4-3/...

    COVERIS

    FDA UDI
    CAMBER SPINE TECHNOLOGIES, LLC·B030CS1021380·Trial,14mm x 16mm Lordotic 7°, 12mm

    Trial Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964081804·Trial Procedure Kit

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964084324·Endo Carry-On Procedure Kit

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964083310·Endo Carry-On Procedure Kit

    SPIRA®-A Integrated

    FDA UDI
    CAMBER SPINE TECHNOLOGIES, LLC·B030SAZ1021380·SPIRA®-A Integrated,Trial, 30x34mm, 25° Lordoti...

    Fixed Reference Posterior ROT Guide 5 deg

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215056469·

    Trial Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964079214·Trial Procedure Kit

    Custom Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964109638·Endo Carry-On Procedure Kit

    PARADIGM SILHOUETTE, MODELS MMT-377, 378, 379, 380

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MODIFICATION TO ACIS (AUTOMATED CELLULAR IMAGING SYSTEM)

    FDA 510(k)
    FDA Class 2 ·Hematology

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964106279·Endo Carry-On Procedure Kit

    ONE TOUCH ULTRA

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·December 19, 2005

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTN·May 9, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·September 19, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 19, 2011

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 17, 2025