BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

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    NASAL SEPTAL BUTTONS

    FDA 510(k)
    FDA Unclassified ·Unknown

    Tranquil-C™

    FDA UDI
    NEXUS SPINE, L.L.C.·B6788226370·Cervical Trial, Thin Shaft, 8x16x13, 6 deg

    Packout-5 - Class A First Aid Kit - Poly

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588226378·Packout-5 - Class A First Aid Kit - Poly

    LITE DECOMPRESSION SYSTEM- LIGHT CABLE MODEL 48089999

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

    BD-3000 MICROKERATOME SYSTEM, MODEL K-3000 MICROKERATOME

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 21, 2014

    INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·November 7, 2012

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC INC.·Product code NKB·August 27, 2010

    Promote Quadra, Sterile EO, Model # / Part #: CD3221-36/100025054, 60019195; CD3223-36P/100013763; CD3239-40/100029115, 100029254, 100037181; CD3239-40Q/100029116, 100029244, 100037115

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