BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    CompactCath Intermittent Urinary Catheter

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

    LATEX POWDERED EXAMINATION GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    LIMA-LIO SMR SHOULDER SYSTEM - HUMERAL STEMS, LIMA-LIO SMR SHOULDER SYSTEM - HUMERAL BODIES,

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    WAVEWRITER ALPHA? PRIME 16

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·September 5, 2025

    BAROUK SCREW - 3 0MM X 32MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HWC·April 7, 2020

    ATTAIN ABILITY

    FDA Adverse Event
    Malfunction ·MPRI·Product code OJX·October 10, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·July 13, 2011

    CXI SUPPORT CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code KRA·August 27, 2020