BEUDAMED
    11 results · 22ms · Sources: EU EUDAMED, US FDA

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    Valleylab REM Polyhesive Infant Patient Return Electrode

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

    ESTEMP NE

    FDA 510(k)
    FDA Class 2 ·Dental

    SHOULDER FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SELEX M2A MAGNUM MODULAR HEAD 40MM HEAD DIAMETER MINUS 6MM NECK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LZO·October 20, 2016

    CARELINK

    FDA Adverse Event
    Malfunction ·RICE CREEK MFG·Product code DXY·June 10, 2013

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·July 13, 2011

    COLLEAGUE 3CX VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 16, 2008

    NON-STERILE KIRSCHNER WIRES AND STEINMANN PINS, MODELS #'S 290-101/160, 290-201/216, 290-060/330, 290-161/220

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PULSAR MAX II MODEL 2800

    FDA Adverse Event
    Injury ·GUIDANT·Product code DXY·July 29, 2005

    AC-GM ESSIX ALIGNER CHEWIE GREEN MINT 20PK

    FDA Adverse Event
    Injury ·DENTSPLY SIRONA ORTHODONTICS INC.·Product code ECS·July 24, 2024

    OT ULTRA2 METER

    FDA Adverse Event
    Injury ·LIFESCAN INC.·Product code NBW·September 26, 2012