BEUDAMED
    10 results · 25ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    VMX MOBILE X-RAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756380300·PACEMAKER ICD PACK

    Gen. Acces/ Instr. Tip Guard

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112359·SURG-I-BAND PURPLE GLOW

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756019873·FINGER SPLINT

    UCR

    FDA UDI
    Seaspine Orthopedics Corporation·10889981080099·Straight Probe

    RH non-Automated Blood Pressure Meter RH non-Automated Blood Pressure Meter with Stethoscope

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEDPOR QUAD MOTILITY IMPLANT

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    EASYTRAK 3

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code OJX·January 11, 2013

    CENTRA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·November 23, 2010

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·July 2, 2014