BEUDAMED
    11 results · 19ms · Sources: EU EUDAMED, US FDA

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    EUGON BROTH

    FDA 510(k)
    FDA Class 1 ·Microbiology

    NA

    FDA UDI
    LANCER ORTHODONTICS, INC.·00817573023417·ULTRA BAND LOK BLUE SYRINGE (5g)

    AIRLIFE HEPA FILTER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    GENESYS SPINE ANTERIOR CERVICAL PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD¿ IV SET SN404 W/O BP Y-CONN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FOZ·May 9, 2019

    APOLLORF? XL90, ASPIRATING ABLATOR 90°

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code GEI·August 6, 2019

    THUNDERBEAT 5 MM, 35 CM, FRONT ACTUATED GRIP

    FDA Adverse Event
    Malfunction ·OLYMPUS MED SYSTEM CORP·Product code GEI·March 24, 2014

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·October 31, 2012

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·August 13, 2010

    BD¿ IV SET SN404 W/O BP Y-CONN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FOZ·April 26, 2019

    HEARTMATE 14 VOLT LITHIUM ION BATTERY SET

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·January 25, 2024