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

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    Biodegradable Nitrile Examination Powder Free Glove, Green

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ECHO BI-METRIC HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304463295·

    Echo® Bi-Metric® Hip System

    FDA UDI
    Biomet Orthopedics, LLC·00887868260575·

    Sonic

    FDA UDI
    Sonic Innovations, Inc.·05711583032610·ET40, KIT 312 NFM L BE ENCHANT 40

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690198420·AK3 Ultra Insert Trial Size 1, 11mm

    MEDICAL MAGNETIC TAPE RECORDER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ENTOMED SCREENING AUDIOMETER, MODEL SA201,SA202, ENTOMED DIAGNOSTIC AUDIOMETER MODEL SA203,SA204

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    OT VERIO2 METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 15, 2015

    OT VERIO2 METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 15, 2015

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NKB·December 7, 2018

    M2A-MAGNUM MOD HD SZ 50MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·September 10, 2015

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·October 7, 2008

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 20, 2013

    VIRTUOSO II VR

    FDA Adverse Event
    Death ·MEDTRONIC MED REL, INC.·Product code LWS·August 4, 2011

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code NKB·November 30, 2020

    36MM I.D. SIZE F NEUTRAL LINER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·May 24, 2022

    CER BIOLOXD MOD HD 32MM STD NK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·October 30, 2018

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code NKB·September 8, 2020

    EPOLY 32MM RNGLC LNR HW SZ24

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·October 30, 2018

    UNIVERSAL INSERTER/EXTRACTOR

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code HWB·June 6, 2017