BEUDAMED
    12 results · 25ms · Sources: EU EUDAMED, US FDA

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    F499 DELUXE ELECTRIC TOOTH BRUSH W/ STAND

    FDA 510(k)
    FDA Class 1 ·Dental

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471122819·K-WIRE - DOUBLE TROCAR 0.6mm DIA x 100mm

    SOFLEX SILICONE SQUARE EDGE IOL

    FDA Adverse Event
    Injury ·BAUSCH & LOMB·Product code HQL·December 9, 2008

    Non-sterile, Powder Free, ambidextrous, textured, beaded cuff, single use, Doffy® Nitrile Examination Glove, Tested for use with Chemotherapy Drugs

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MERIT HYDROPHILIC GUIDE WIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    X-FLOW PROSTATECTOMY CATHETER

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code EZL·February 28, 2025

    STELLARIS 25GA POSTERIOR PACK W AFI AND FF 6/BX

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB, INC.·Product code HQC·October 28, 2014

    STELLARIS 25GA POSTERIOR PACK W AFI AND FF 6/BX

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB, INC.·Product code HQC·October 28, 2014

    STELLARIS 25GA POSTERIOR PACK W AFI AND FF 6/BX

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB, INC.·Product code HQC·October 28, 2014

    CONCERTO CRT-D DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code NIK·December 13, 2010

    CONFIRM

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code MXC·July 8, 2014

    TOTALCARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·December 10, 2012