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

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    APR FULLY TEXTURED HIP STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471149854·K-WIRE - DOUBLE TROCAR FULLY THREADED 1.8mm DIA...

    WECK-KREEM, CATALOG NO. 850-155

    FDA 510(k)

    SOLARC / SOLRX HANDHELD ULTRAVIOLET PHOTOTHERAPY LAMP UNIT FAMILY

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR PURITAN·Product code CBK·February 11, 2013

    HEARTMATE II SYSTEM CONTROLLER, EU

    FDA Adverse Event
    Malfunction ·THORATEC CORP.·Product code DSQ·December 27, 2010

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 28, 2014

    FT3 - FREE TRIIODOTHYRONINE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CDP·July 21, 2014

    TSH, THYROTROPIN

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JLW·May 20, 2014

    FT3 - FREE TRIIODOTHYRONINE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CDP·April 30, 2014

    TSH, THYROTROPIN

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JLW·April 9, 2014

    TSH, THYROTROPIN

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JLW·March 24, 2014

    EVOLIS MICROPLATE SYSTEM

    FDA Adverse Event
    Malfunction ·BIO-RAD LABORATORIES, INC.·Product code MZF·October 23, 2009