BEUDAMED
    37 results · 23ms · Sources: EU EUDAMED, US FDA

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    LC Bead LUMI

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Simpact Tri-Fin

    FDA UDI
    Life Spine, Inc.·00190837062972·Steinmann Pin Caddy, Long Trocar Pins

    Trial Liners (Neutral and 10 degree hooded)

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215038434·

    INNOVA CT OPTION FOR DIGITAL FLUOROSCOPIC IMAGING SYSTEMS INNOVA MODELS 4100, 4100IQ, 3100, 3100IQ & 2100IQ

    FDA 510(k)
    FDA Class 2 ·Radiology

    ELECSYS PRECICONTROL MULTIMARKER

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    QUICK-CORE ULTRASOUND BIOPSY NEEDLE

    FDA Adverse Event
    Injury ·COOK ENDOSCOPY·Product code FCG·September 4, 2018

    APPLIANCE,FIXATION,SPINAL INTERVERTEBRAL BODY

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code KWQ·November 10, 2015

    APPLIANCE,FIXATION,SPINAL INTERVERTEBRAL BODY

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code KWQ·November 10, 2015

    SPINAL VERTEBRAL BODY REPLACEMENT DEVICE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MQP·November 10, 2015

    APPLIANCE,FIXATION,SPINAL INTERVERTEBRAL BODY

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code KWQ·November 10, 2015

    APPLIANCE,FIXATION,SPINAL INTERLAMINAL

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code KWP·November 10, 2015

    URETEX TO2 URETHRAL SUPPORT SYSTEM

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code OTN·May 24, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·July 7, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 8, 2014

    KYPHON BONE CEMENT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NDN·April 23, 2019

    MOSAIC MITRAL BIOPROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·January 3, 2018

    MOSAIC MITRAL BIOPROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·January 3, 2018

    NA

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code DYE·January 3, 2018

    1030489-2019-01423

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NDN·December 13, 2019

    MEDTRONIC LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DXY·February 21, 2020