BEUDAMED
    12 results · 30ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Disposable SpO2 Sensors, Reusable SpO2 Sensors

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PILLING

    FDA UDI
    TELEFLEX INCORPORATED·24026704512670·

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515025448·Langenbeck Retr, fenes hndl, 30x11mm, 8 1/4"

    REUSABLE STIMULATING ELECTRODES

    FDA 510(k)
    FDA Class 2 ·Neurology

    SWABFLSUH (3ML, 5ML, 10ML) MODEL 10331, 10351, 10311

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 25, 2024

    HELICAL BLADE COUPLING SCREW

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code LXH·October 17, 2014

    UNK

    FDA Adverse Event
    Malfunction ·ST JUDE MED - NEUROMODULATION·Product code LGW·July 8, 2011

    SIGMA STAB GVF INS 2 15MM

    FDA Adverse Event
    Injury ·1219655 DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDIC·Product code JWH·June 21, 2013

    INTRAUTERINE ACCESS BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LKF·December 10, 2020

    ALK (D5F3)

    FDA Adverse Event
    Malfunction ·VENTANA MEDICAL SYSTEMS INC.·Product code NJT·August 22, 2025

    SELECTIVE SALPINGOGRAPHY CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LKF·November 19, 2021