BEUDAMED
    7 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    PHENOBARBITAL FLEX REAGENT CARTRIDGE

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    SUTURE REMOVAL KIT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MALT AGAR

    FDA 510(k)
    FDA Class 1 ·Microbiology

    BD BBL¿ MGIT¿ OADC ENRICHMENT

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·May 13, 2024

    S-ROM M HEAD 36MM +6

    FDA Adverse Event
    Malfunction ·DEPUY INTERNATIONAL·Product code JDI·February 6, 2013

    TELIGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·January 3, 2011

    SPACELABS TELEMETRY RECEIVER MODULE

    FDA Adverse Event
    Malfunction ·SPACELABS HEALTHCARE INC.·Product code DSI·July 18, 2014