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

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    BOUNDER 300 Power Wheelchair, BOUNDER Plus 300 Power Wheelchair, BOUNDER 450 Power Wheelchair, BIG BOUNDER 600 Power Wheelchair, BIG BOUNDER 1000 Power Wheelchair

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    UNIVERSAL DIGITAL INTERFACE (UDI) 1717

    FDA 510(k)
    FDA Class 2 ·Radiology

    ARROW ANATOMICAL SHOULDER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NEXTAR INFRARED CAMERA

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code JWH·September 10, 2021

    MIRU 1DAY UPSIDE (MIDAFILCON A)

    FDA Adverse Event
    Injury ·MENICON CO., LTD.·Product code LPL·January 22, 2025

    UNK

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 25, 2013

    OPTISENSE

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, CRMD·Product code DTB·January 13, 2014

    MPS DELIVERY SET W/ARREST AGENT, ADDITIVE CASS

    FDA Adverse Event
    Malfunction ·QUEST MEDICAL·Product code DTR·July 14, 2011

    INDIGO SYSTEM ASPIRATION CATHETER 7D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code QEW·December 10, 2024

    INDIGO SYSTEM ASPIRATION CATHETER 7D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code QEW·January 5, 2023