BEUDAMED
    7 results · 21ms · Sources: EU EUDAMED, US FDA

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    SUNDT-KEES REINFORCING ANEURYSM CLIP

    FDA 510(k)
    FDA Class 2 ·Neurology

    ADULT VENT CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CIN-SHEAR

    FDA 510(k)
    FDA Class 1 ·Obstetrics/Gynecology

    FLASH Ostial System, Dual Balloon Angioplasty Catheter, REF: OAB6014BA

    FDA Recall
    Terminated ·Ostial Corporation·Product code LIT·July 14, 2021

    PNEUMO SURE HIGH FLOW INSUFFLATOR W/ SIDNE (EU1)

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code HIF·June 2, 2014

    GALILEO ECHO

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·November 26, 2012

    TANDEM T:SLIM INSULIN DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE INC.·Product code LZG·June 12, 2015