BEUDAMED
    8 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.

    CHARLES/MCINTYRE GIANT BREAK TABLE

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

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377020901·RELINE-C Ti Rod, 3.5x115mm Straight

    NA

    FDA UDI
    STRYKER CORPORATION·07613327055306·2.0 Fr., Short-tip Electrode, Do not use if pac...

    GII QUICKANCHOR PLUS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SV Spectrum MRC Central Venous Catheter; SV Spectrum MR Central Venous Catheter; SV Central Venous Catheter

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MAQUET HCU30 DEVICE

    FDA Adverse Event
    Injury ·MAQUET CARDIOPULMONARY AG·Product code DWC·May 16, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 21, 2012

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·September 17, 2010