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

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    BRK TRANSSEPTAL NEEDLE MODEL 407200, 407201, 407205, 407206, 407207, G407208

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    WAVEWRITER ALPHA 16

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 31, 2023

    MEDTRADE PRODUCT'S ANTISEPTIC BARRIER HYDROGEL DRESSINGS

    FDA 510(k)
    FDA Unclassified ·Unknown

    LLX240AB01

    FDA 510(k)
    FDA Class 2 ·Radiology

    DISP BIPOLAR FORCEPS CORD

    FDA Adverse Event
    Injury ·COVIDIEN LP·Product code GEI·May 17, 2013

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·September 18, 2014

    RELIA SR

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code NVZ·June 14, 2011

    Exactech Equinoxe CAGE GLENOID,POSTERIOR AUGMENT, CEMENTED, Left, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-13-22, b) 41, 44, 47, 50, head, Medium, Item Number 314-13-23, c) 44, 47, 50, 53 head, Large, Item Number 314-13-24, d) 44, 47, 50, 53 head, Extra Large, Item Number 314-13-25; Shoulder Arthroplasty

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·April 10, 2024