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

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    APPLICARD (EKG)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    URINE BARBITURATES (BARB) SCREEN FLEX REAGENT CARTRIDGE, CATALOG NO. DF 96A

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    DISPOSABLE TPE INFUSION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MASUNAGA since 1905

    FDA UDI
    MASUNAGA OPTICAL MFG.CO.,LTD.·04582644465231·

    DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM

    FDA Adverse Event
    Injury ·NIPRO CORPORATION *USD*·Product code KDI·June 27, 2014

    TERUMO STERNAL SAW II

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code GFA·October 28, 2010

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·January 7, 2013