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

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    AQUAPAK 020 HUMIDIFIER ADAPTER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    UNKNOWN BUR

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code EQJ·November 4, 2020

    UNKNOWN BUR

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code EQJ·November 4, 2020

    UNKNOWN BUR

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code EQJ·November 4, 2020

    UNKNOWN BUR

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code EQJ·November 4, 2020

    VARIAX DISTAL RADIUS PLATING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HERMES BOND

    FDA 510(k)
    FDA Class 2 ·Dental

    XPS® BUR - UNKNOWN

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code EQJ·March 9, 2017

    DRILL 3055601 SKEETER OTO-TOOL

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC·Product code ERL·January 11, 2013

    XPS® BUR - UNKNOWN

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code EQJ·March 8, 2017

    EDM LUMBAR DRAINAGE KIT, OPEN TIP CATHETER

    FDA Adverse Event
    Death ·MEDTRONIC NEUROSURGERY·Product code GWM·May 27, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·November 9, 2012

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·August 31, 2010