BEUDAMED
    9 results · 32ms · Sources: EU EUDAMED, US FDA

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    XELERIS 3 PROCESSING AND REVIEW WORKSTATION

    FDA 510(k)
    FDA Class 2 ·Radiology

    TEMPERATURE FUNCTION, MODEL 9500 MULTIGAS MONITOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    2008T HEMODIALYSIS SYS., WITH CDX

    FDA Adverse Event
    Malfunction ·CONCORD MANUFACTURING·Product code KDI·June 26, 2018

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·May 6, 2013

    PRIMEADVANCED

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·September 16, 2014

    SMART MONITOR 2

    FDA Adverse Event
    Other ·PHILIPS RESPIRONICS, INC.·Product code FLS·April 27, 2011

    SORIN AF 620 W/LOOP 10

    FDA Adverse Event
    Other ·SORIN GROUP USA, INC.·Product code DWE·June 25, 2010

    BD MICROTAINER® MAP MICROTUBE FOR AUTOMATED PROCESS K2 EDTA

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code JKA·July 3, 2019