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

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    COPPER KETTLE VAPORIZER PLUS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704292732·

    NA

    FDA UDI
    KEY SURGICAL, INC.·10849771049071·K-Wires, Single trocar, .028-inch (.7mm) diamet...

    Key Surgical K-Wires and Steinmann Pins

    FDA UDI
    KEY SURGICAL, INC.·00849771012498·K-Wires, Single trocar, .028-inch (.7mm) diamet...

    Ankle Compression Nailing System

    FDA UDI
    ORTHOFIX SRL·18033509858376·TITANIUM ANKLE COMPRESSION NAIL 11/150

    AW-100

    FDA 510(k)
    FDA Class 2 ·Dental

    TROCAR VENTILATION TUBE/WITH TROCAR TIP, TROCAR HANDLE, MODEL 1015 074, 1015 076, 1015 075, 1015 077, W/ RETENTION WIRE

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    HUDSON UP-DRAFT II OPTI-NEB NEBULIZER W/RESERV

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code CAF·January 22, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·October 3, 2012

    COULTER® LH 780

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·July 27, 2010

    SIRIUS HIP STEM 44-D

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·June 23, 2023

    Allura Exper FD Series. System codes 722003 722010 722022 722005 722011 722019 722001 722002 722006 722012 722008 722013 722020 722025 722015 722023 722038 889006 889016 889009 722005 The device is an X-Ray Generator.

    FDA Enforcement
    Class II ·Terminated·Philips North America, LLC·March 25, 2020