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

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    KINEMAX PLUS ALL PLASTIC TIBIAL COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123267·K-WIRE - DOUBLE TROCAR 1.6mm DIA x 100mm

    ZIMMER PATIENT SPECIFIC INSTRUMENTS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HANSATOME EXCELLUS MICROKERATOME

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    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

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 10, 2013

    6800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 7, 2010

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·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

    UNKNOWN IMPACTOR

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code HWA·April 12, 2021

    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