BEUDAMED
    17 results · 21ms · Sources: EU EUDAMED, US FDA

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    GK DENTAL AMALGAM ALLOY

    FDA 510(k)
    FDA Class 2 ·Dental

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111086·INSTRUMENT CASE LARGE ALUMINUM

    PICCOLO HDL TEST SYSTEM

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    TX1 TISSUE REMOVAL SYSTEM

    FDA 510(k)
    FDA Unclassified ·Unknown

    LARGE AO COUPLING ASNIS III HALL FITTING

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·September 25, 2012

    ENDOTRACHEAL TUBE 7.5 MM EMG FLEX

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code BTR·July 28, 2010

    MAINFRAME 8253001 NIM RESPONSE 3.0

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC·Product code ETN·December 16, 2013

    MODULAR CATHCART BALL 48MM OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LZY·December 9, 2010

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 22, 2013

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code IOR·July 9, 2014

    ENDOTRACH TUBE 8229306J NIM EMG 6MM

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC·Product code ETN·March 6, 2013

    ENDOTRACHEAL TUBE 8229307 NIM EMG 7MM RE

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code ETN·May 10, 2013

    ENDOTRACH TUBE 8229980 5PK 8MM EMG FLEX

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code ETN·March 11, 2013

    MAINFRAME 8253001 NIM RESPONSE 3.0

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code ETN·August 26, 2013

    ENDOTRACH TUBE 8229980 5PK 8MM EMG FLEX

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code ETN·February 11, 2013

    NIM® EMG - ENDOTRACHEAL TUBE - NIM FLEX¿

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED INC.·Product code ETN·October 18, 2021

    MAINFRAME 8253001 NIM RESPONSE 3.0

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code ETN·August 28, 2013