BEUDAMED
    8 results · 27ms · Sources: EU EUDAMED, US FDA

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    EVITA 4 (8411900)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    UNKNOWN SCREW

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code PAO·February 4, 2015

    COMPREHENSIVE REVERSE SHOULDER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Pro-Link® Ti Stand-Alone Cervical Spacer System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LIFEVEST WCD 3100 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·June 20, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 27, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·February 7, 2011

    COPELAND THN SHL COCR/HA HUMS3

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWS·August 28, 2025