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

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    Amplatzer Trevisio Intravascular Delivery System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172971314·

    PROPATCH SOFT TISSUE REPAIR MATRIX

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

    TANTALUM BEAD SET, MODEL P003175

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

    ENDURANT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·June 26, 2013

    ADVANTA

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·October 2, 2008

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·July 27, 2011

    VASERLIPO SYSTEM

    FDA Adverse Event
    Injury ·SOLTA MEDICAL, INC·Product code QPB·January 5, 2023

    AEQUALIS STEM FOR FRACTURE D.6.5 HA-COATED

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code KWS·January 5, 2026

    VASERLIPO SYSTEM

    FDA Adverse Event
    Injury ·SOLTA MEDICAL, INC·Product code QPB·January 10, 2023

    VASERLIPO SYSTEM

    FDA Adverse Event
    Injury ·SOLTA MEDICAL, INC·Product code QPB·October 21, 2022