BEUDAMED
    12 results · 28ms · Sources: EU EUDAMED, US FDA

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    EXTERNAL FIXATOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111062·INSTRUMENT CASE MEDIUM ALUMINUM

    Ophthalmic Forceps

    FDA UDI
    KATENA PRODUCTS, INC.·00841668106273·KELMAN-MCPHERSON FORCEPS 1X2 TEETH

    Expression MR400 MRI Patient Monitoring System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TRU-SWAB STOCOCK

    FDA 510(k)
    FDA Class 2 ·General Hospital

    M2A 38MM MOD HD -3MM NK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 19, 2018

    TAPERLOC POR FMRL 13.5X147

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·June 25, 2018

    M2A 38MM MOD HD -3MM NK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·June 25, 2018

    TAPERLOC POR FMRL 13.5X147

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 19, 2018

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·December 30, 2010

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·February 9, 2013

    ESSURE

    FDA Adverse Event
    BAYER PHARMA AG·Product code HHS·July 18, 2014