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

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    MK 808 SERIES NASAL OXYGEN SAMPLER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SeaSpine Expandable Interbody

    FDA UDI
    Seaspine Orthopedics Corporation·10889981123499·IMPLANT, 26mm LG, 8-12mm HT, 10mm WD, 0 DEG

    Integra Expandable Interbody

    FDA UDI
    Seaspine Orthopedics Corporation·10889981049270·IMPLANT, 26mm LG, 8-12mm HT, 10mm WD, 0 DEG. Th...

    Legacy

    FDA UDI
    Gc Orthodontics America Inc.·E53582260800001·LEGACY 1. MOLAR UPR LFT SZ 08

    Tuttnauer Pre-vacuum Steam Sterilizer models 3870HSG and 3870HSG-WS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    HEMATIC BLOOD MIXER

    FDA 510(k)
    FDA Class 1 ·Hematology

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·December 12, 2017

    PROXIMATE ILS STRAIGHT INTRALUMINAL STAPLER - 29MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code GDW·November 27, 2007

    MONOPOLAR CAUTERY INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·November 7, 2012

    OT VERIO IQ METER

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

    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