BEUDAMED
    16 results · 20ms · Sources: EU EUDAMED, US FDA

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    MFP-051

    FDA 510(k)
    FDA Class 2 ·Dental

    OPTICROSS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OBJ·August 22, 2025

    OPTICROSS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OBJ·September 23, 2025

    ASTRA TECH DENTAL IMPLANTS-CERAMIC ABUTMENTS

    FDA 510(k)
    FDA Class 2 ·Dental

    SLEEPMINDER BREATHING FREQUENCY INDICATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970720·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970737·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970744·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172973387·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970706·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970713·

    GUIDANT VITALITY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code LWS·May 9, 2013

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·September 26, 2014

    MAGELLAN BC 21G X 1.25"

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FMI·June 10, 2011

    SENSITHERM PROBE

    FDA Adverse Event
    Injury ·FIAB S.P.A.·Product code FLL·July 10, 2023

    TOSOH ST AIA 25-OH VITAMIN D PRETREATMENT SET

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code MRG·April 19, 2018