BEUDAMED
    71 results · 30ms · Sources: EU EUDAMED, US FDA

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    FUNNEL ADAPTOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111055·SILICONE MAT FOR K 9-2320

    RMGI LOW VISCOSITY

    FDA 510(k)
    FDA Class 2 ·Dental

    CryoX Vitrification Freeze Kit / Thaw Kit

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    HOMECHOICE, DOMESTIC 120V

    FDA Adverse Event
    BAXTER HEALTHCARE·Product code FKX·June 11, 2008

    HOMECHOICE, DOMESTIC 120V

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·July 24, 2009

    PD CYCLER 110 VOLT HOME CHOICEPRO AUTOMATED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·June 18, 2008

    HOMECHOICE CYCLER-REFURBISHED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·December 4, 2007

    HOMECHOICE CYCLER-REFURBISHED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·December 10, 2007

    PD CYCLER 110 VOLT HOME CHOICEPRO AUTOMATED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·June 18, 2008

    PD CYCLER 110 VOLT HOME CHOICEPRO AUTOMATED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·June 27, 2008

    PD CYCLER 110 VOLT HOME CHOCIEPRO AUTOMATED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·June 18, 2008

    PD CYCLER 110 VOLT HOME CHOICEPRO AUTOMATED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·June 18, 2008

    HOMECHOICE CYCLER-REFURBISHED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·May 13, 2008

    HOMECHOICE CYCLER -REFURBISHED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·June 5, 2008

    HOMECHOICE CYCLER REFURBISHED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·March 6, 2008

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 13, 2010

    CORE UNIVERSAL DRIVER

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code ERL·July 9, 2014

    RADIOFREQUENCY ABLATION GENERATOR

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code JOS·April 3, 2006

    HOMECHOICE CYCLER-REFURBISHED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·May 14, 2008