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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    ONE STEP MORPHINE CARD TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970579·anteriors; shade BL4; mould UIS

    CATHETER, URETHRAL PRESSURE, UPE-10 & 12

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    STORZ SLX-F2 STORM TOUCH

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PUMP IN STYLE ADVANCED BREAST PUMP GO TOTE

    FDA Adverse Event
    Malfunction ·MEDELA, INC.·Product code HGX·June 2, 2014

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·February 20, 2013

    COAGUCHEK® S SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JPA·January 25, 2011