BEUDAMED
    8 results · 34ms · Sources: EU EUDAMED, US FDA

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    IMED 4100 AND 4200 DISPOSABLE INFUSION DEVICES MOD

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MODIFICATION TO REFLECTION CROSS-LINKED UHMWPE ACETABULAR COMPONENTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AMPLATZER VASCULAR PLUG 4

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    IROX

    FDA Adverse Event
    Injury ·GUIDANT ANGLETON/ST. PAUL·Product code NVN·January 14, 2013

    8800

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD·Product code JAA·November 12, 2010

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·July 3, 2014

    PHYSICA KR TIB. LINER RIGHT #4

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code JWH·June 11, 2024

    DEKA SMARTPERIO

    FDA Adverse Event
    Injury ·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code NVK·December 11, 2024