BEUDAMED
    11 results · 20ms · 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.

    OHMEDA - LOW FLOW FLOWMETER

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756350549·LAPAROTOMY PACK

    neoWave LS

    FDA UDI
    XENIX MEDICAL LLC·00818345024113·Paddle Shaver, 16mm

    InTess Lumbar Cage

    FDA UDI
    Kalitec Direct LLC·B07312K0103160·Shaver, Closed, 16mm

    WARMTOUCH COMPACT WARMING UNIT

    FDA Adverse Event
    Malfunction ·COVIDIEN/FORMERLY TYCO·Product code DWJ·December 23, 2010

    COOLTOUCH VARIA ND:YAG LASER SYSTEM; COOLTOUCH VARIA-II ND:YAG LASER SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    INFOSEND GSM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    WARM TOUCH II COMPACT WARMING UNIT

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY TYCO HEALTHCARE·Product code DWJ·September 24, 2010

    ACUITY

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

    PRODISC-C(TM) IMPLANT MEDIUM

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MJO·November 23, 2010

    SPIDERFX EMBOLIC PROTECTION DEVICE

    FDA Adverse Event
    Injury ·COVIDIEN·Product code NTE·July 2, 2014