BEUDAMED
    36 results · 24ms · Sources: EU EUDAMED, US FDA

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    AMEDITECH IMMUTEST MILTI-DRUG SCREEN

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Comprehensive® Shoulder System

    FDA UDI
    Biomet Orthopedics, LLC·00880304212244·

    CapSure® Spine System

    FDA UDI
    Spine Wave, Inc.·10840642104028·Rod Curved 5.5 x 45mm

    Comprehensive Shoulder System

    FDA UDI
    Biomet Orthopedics, LLC·00880304681088·

    COSMOS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HOSMAN USB BLOOD PRESSURE MONITOR; WRIST TYPE AND UPPER ARM TYPE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 9, 2025

    LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KTT·October 19, 2012

    LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KTT·October 19, 2012

    LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KTT·October 19, 2012

    LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KTT·October 19, 2012

    EON MINI

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 10, 2013

    LAMITRODE S8

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·September 17, 2014

    MINI TREK CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LOX·June 3, 2011

    COMP RVRS SHLDR GLNSP +6 36MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·March 24, 2021

    SM HYBRID GLENOID BASE 4MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·September 1, 2021

    PC HYBRID GLEN POST- POLY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·September 1, 2021

    COMPREHENSIVE PT HYBRID GLEN POST REGENEREX

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·November 11, 2019

    U BY KOTEX SLEEK

    FDA Adverse Event
    Malfunction ·K-C AFC MANUFACTURING, S. DE R.L. DE C.V·Product code HEB·August 31, 2018

    COMPREHENSIVE VERSA-DIAL 46X24X47 HUMERAL HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBF·September 6, 2018