BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    CURA COLLIMATOR

    FDA 510(k)
    FDA Class 2 ·Radiology

    TRABIS [K173893]

    FDA Adverse Event
    Injury ·COLIGNE AG·Product code PLR·April 23, 2019

    ST AIA-PACK CEA ENZYME IMMUNOASSAY

    FDA 510(k)
    FDA Class 2 ·Immunology

    IMAGER II ANGIOGRAPHIC CATHETERS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 23, 2024

    LIFEGUARD HUBER NEEDLE SET

    FDA Adverse Event
    Malfunction ·VYGON MANUFACTURING·Product code FPA·May 15, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 27, 2014

    SECURA DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·June 14, 2011