BEUDAMED
    22 results · 22ms · Sources: EU EUDAMED, US FDA

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    M VISUM ALERT ALARM MANAGEMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517636041·CoRoent Ant TLIF PEEK, 11x12x28mm 12°

    9300

    FDA UDI
    HANS RUDOLPH, INC.·00874750008438·9326 INSP OCCL 9300/2600/9301

    STERILE POWDER FREE SYNTHETIC VINYL PATIENT EXAM GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    THE VARIA FIBULA LOCKED PLATING SYSTEM LINE EXTENSION ADDITION OF STRAIGHT PLATES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·January 23, 2019

    LINEAR ST

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·January 2, 2023

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·April 23, 2026

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·April 23, 2026

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·April 24, 2026

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·April 23, 2026

    UNK

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code PHX·April 23, 2026

    UNK

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code PHX·April 23, 2026

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·April 23, 2026

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·April 23, 2026

    IN TOUCH ZU

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·April 29, 2011

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·May 14, 2013

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code IOR·September 23, 2014

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·April 23, 2026

    ANGIOSCULPT PTA SCORING BALLOON CATHETER (OTW)

    FDA Adverse Event
    Malfunction ·ANGIOSCORE, INC·Product code LIT·November 18, 2015