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

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    I-HIP TOTAL HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Bernafon

    FDA UDI
    Bernafon AG·05711584050859·CA5 ITED, WL R BE CARISTA 5

    INTERACTIVE SBM 3.7MMDX13MML 3.0MM PLAT

    FDA Adverse Event
    Injury ·IMPLANT DIRECT SYBRON MANUFACT·Product code DZE·October 29, 2025

    IYUNNI 3ID SUPRAPUBIC CYSTOSTOMY TUBE KIT

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    A-DEC/W&H ELECTRIC MOTOR, MODEL EA-50LT

    FDA 510(k)
    FDA Class 1 ·Dental

    2132572-1999-00044

    FDA Adverse Event
    Malfunction ·December 30, 1999

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES(USA)·Product code HRS·May 15, 2014

    FLEXOR RADIAL ACCESS SET

    FDA Adverse Event
    Injury ·COOK, INC.·Product code DYB·April 13, 2015

    INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 1, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013

    6.5 CANCELLOUS BONE SCREW 30MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code HWC·June 10, 2011

    FLEXOR RADIAL ACCESS SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DYB·July 12, 2016