BEUDAMED
    11 results · 18ms · 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.

    WORRELL TRIAL PATELLA

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704293968·

    Key Surgical K-Wires and Steinmann Pins

    FDA UDI
    KEY SURGICAL, INC.·00849771015239·Steinmann Pins, Single diamond, threaded, 1/8-i...

    NA

    FDA UDI
    KEY SURGICAL, INC.·10849771050039·Steinmann Pins, Single diamond, threaded, 1/8-i...

    Young Specialties

    FDA UDI
    Young Innovations, Inc.·00843471188842·.022 L/L MBT STD. WELD SIZE #9

    ARTHROCARE SYSTEM 12000

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

    BR-FHUS Viewer 1.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    GENTEEL HOMECARE PRODUCTS·Product code ITJ·April 24, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 4, 2012

    STERLING ES PTA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LIT·July 28, 2010

    Unify, Sterile EO, Model #/ Part #: CD3231-40/100029240, 100030104, 100041904; CD3231-40Q/100029281, 100030124, 100041905; CD3235-40/100029256, 100029293, 100029307, 100031111, 100037047, 100048897, 100070009; CD3235-40Q/100029257, 100029294, 100029308, 100031059, 100037048, 100070010; CD3281-40Q/100056770; CD3297-40/100056933

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018