BEUDAMED
    11 results · 18ms · Sources: EU EUDAMED, US FDA

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    RITE-BITE BIOPSY FORCEPS

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756049917·Stockinette

    CT Expres 3D Contrast Media Delivery System, Bottle Spike Type B, Day Set III HP, Patient Set

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SURGISIS STAPLE LINE REINFORCEMENT II

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    IMPELLA CP

    FDA Adverse Event
    Malfunction ·ABIOMED, INC.·Product code OZD·December 26, 2025

    Stockinette, Single Ply, Standard Weave, 8 X 72'' and 10 X 48'', Ref #9508-72, #9510-48, #9510-48, #9510-60

    FDA Recall
    Terminated ·Product code KKX·September 9, 2004

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·February 8, 2013

    CONTAK RENEWAL

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·January 6, 2011

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 22, 2014

    LOGIC TIBIA PS MOD INSRT SZ 5 15MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·July 19, 2023

    LOGIC FEMORAL PS CEM RIGHT SZ 5

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·December 2, 2024