BEUDAMED
    9 results · 26ms · Sources: EU EUDAMED, US FDA

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    ACS PHENOBARBITAL

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Spinous Process System

    FDA UDI
    Seaspine Orthopedics Corporation·10889981096205·Compressor, Spinous Process Spacer

    iNSitu™ Hip System

    FDA UDI
    NEXTSTEP ARTHROPEDIX, LLC·00816127023309·Slap Hammer

    Fingertip Pulse Oximeter A310

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ESTECH CLEARVIEW MV ATRIAL DEPRESSOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    METRX SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HRX·June 10, 2024

    ELECTRODE, PACEMAKER, PERMANENT

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·February 9, 2013

    HOMECHOICE CYCLER-REFURBISHED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·January 7, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 23, 2014