BEUDAMED
    9 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    BURNFREE PAIN RELIEVING GEL, MODEL 4B

    FDA 510(k)
    FDA Unclassified ·Unknown

    Eargo RX

    FDA UDI
    Eargo, Inc.·00850010429274·Eargo SE-Rx New System

    Monaco RTP System

    FDA 510(k)
    FDA Class 2 ·Radiology

    ATTRIUS, MODEL PET150A6001, ATTRIUS L, MODEL PET150A8001, TRUESIGHT, MODEL NSP-P6C, TRUESIGHT, MODEL NSP-P8

    FDA 510(k)
    FDA Class 2 ·Radiology

    MONACO

    FDA Adverse Event
    Malfunction ·ELEKTA INC.·Product code MUJ·July 28, 2021

    ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION CORP·Product code FRN·February 6, 2013

    ENTRUST AT

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·February 15, 2011

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·August 7, 2014

    MONACO

    FDA Adverse Event
    Malfunction ·ELEKTA INC·Product code MUJ·August 25, 2021