BEUDAMED
    13 results · 30ms · Sources: EU EUDAMED, US FDA

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    ExactVu High Resolution Micro-Ultrasound System

    FDA 510(k)
    FDA Class 2 ·Radiology

    BI-METRIC HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304254787·

    PRECINORM CK-MB AND PRECIPATH CK-MB CONTROLS

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    LIFEPAK 12

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code LDD·December 4, 2012

    LIFEPAK® 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·February 6, 2019

    UNKNOWN PLATE

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·April 21, 2026

    UNKNOWN PLATE

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·April 21, 2026

    UNKNOWN PLATE

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·April 21, 2026

    LIFEPAK(R) 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·October 25, 2019

    SPRINT QUATTRO SECURE S MRI SURESCAN

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·October 10, 2014

    PROXIMATE** SKIN STAPLER 35 WIDE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDT·July 15, 2011

    CONSTELLATION LXT VISION SYSTEM

    FDA Adverse Event
    ALCON·Product code HQC·May 8, 2013