BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    COOL-LITE FIBERCOPTIC LARYNGEAL EXAM

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    EVA EMPTY SOLUTION CONTAINER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SONOPULSE/ SONOPULSE III

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    NEURON DELIVERY CATHETER 070

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DQY·March 15, 2010

    MARYLAND BIPOLAR FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·May 23, 2014

    DYNASTY(R) A-CLASS(R) POLY LINER

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LPH·November 13, 2012

    Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026

    Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564, CD3255-40/100038224, CD3255-40Q/100036514

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