BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    BURNSHIELD FIRE BLANKET

    FDA 510(k)
    FDA Class 1 ·General Hospital

    FULLY AUTOMATIC WIRELESS BLOOD PRESSURE WRIST MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SEER LIGHT COMPACT DIGITAL HOLTER RECORDER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK ENDOSCOPY·Product code KGE·April 4, 2017

    COMPREHENSIVE REVERSE SHOULDER CENTRAL SCREW

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWS·April 13, 2017

    KEEPSAFE DELUXE

    FDA Adverse Event
    Malfunction ·J. T. POSEY CO.·Product code KMI·May 20, 2014

    UNK ZIMMER TRILOGY SHELL

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code LPH·January 9, 2013

    ATTAIN OTW

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 13, 2010

    Philips Zenition 50, Model Number: 718096

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·November 20, 2024