BEUDAMED
    9 results · 26ms · Sources: EU EUDAMED, US FDA

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    SEALFLEX MASK

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    SURGICAL INSTRUMENT TRAY

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    TRACHEAL TUBE W/AIRWAY INTUBATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ACUMATCH GXL 15DEG LINER 32MM SZ G

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·December 19, 2023

    TDX/TDXFLX CANNABINOIDS REAGENT

    FDA Adverse Event
    Injury ·ABBOTT HEALTH PRODUCTS, INC.·Product code LDJ·November 8, 2006

    LOGIC TIBIA PS MOD INSRT SZ 4 15MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·August 5, 2022

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 24, 2014

    INTRINSIC

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code LWS·October 19, 2010

    ASR TAP SLV ADAP 12/14 -1

    FDA Adverse Event
    Malfunction ·DEPUY INTERNATIONAL·Product code KWA·December 16, 2012