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

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    HARGIS SR2 SELF-RETRACTION SYSTEM

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    PAQ.210X300X200*28*ESAOTE-FOR

    FDA UDI
    AB MEDICA GROUP, S.A.·08428763009542·

    WRIST FIT

    FDA UDI
    Stryker GmbH·00886385000107·Ulnar Column Plate

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110928·STERILIZING CASE SINGLE VR

    CAPNOGRAPHY PAD (92516)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    LEESPEC DISPOSABLE VAGINAL SPECULUM

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·January 17, 2013

    TERUMO CDI 500 BLOOD PARAMETER MONITOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·November 11, 2010

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 9, 2014