BEUDAMED
    28 results · 27ms · Sources: EU EUDAMED, US FDA

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    ELLIPSE MAGEC SPINAL BRACING AND DISTRACTION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MAGEC SPINAL BRACING AND DISTRACTION SYSTEM

    FDA Adverse Event
    Injury ·ELLIPSE TECHNOLOGIES, INC.·Product code PGN·June 23, 2014

    MAGEC SPINAL BRACING AND DISTRACTION SYSTEM

    FDA Adverse Event
    Injury ·ELLIPSE TECHNOLOGIES, INC.·Product code PGN·May 25, 2014

    MAGEC SPINAL BRACING AND DISTRACTION SYSTEM

    FDA Adverse Event
    Injury ·ELLIPSE TECHNOLOGIES, INC.·Product code PGN·May 21, 2014

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981193874·Interbody, 11mm x 40mm x 17mm, 8 deg

    Reef TH

    FDA UDI
    Seaspine Orthopedics Corporation·10889981201869·Interbody, 11mm x 40mm x 17mm, 8 deg

    ESTELITE COLOR

    FDA 510(k)
    FDA Class 2 ·Dental

    PULSEOX 5500 FINGER DEVICE, PULSEOX 7500 WRISTWATCH DEVICE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RADICAL-7 HANDHELD

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

    RADICAL-7 HANDHELD

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

    RADICAL-7 HANDHELD

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

    RADICAL-7 HANDHELD

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

    RADICAL-7 HANDHELD

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

    RADICAL-7 HANDHELD

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

    RADICAL-7 HANDHELD

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·November 18, 2014

    RADICAL-7

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·February 19, 2016

    K-WIRE

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code HWC·December 9, 2016

    SEDLINE KIT

    FDA Adverse Event
    Malfunction ·MASIMO - 40 PARKER·Product code MWI·January 8, 2017

    TRUEBALANCE

    FDA Adverse Event
    Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code NBW·May 29, 2013

    IMMAGE® RHEUMATOID FACTOR (RF) REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code DHR·June 25, 2011