BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    HEMOCCULT® ICT TEST DEVICE

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

    HEMOCCULT® ICT TEST DEVICE

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

    HEMOCCULT® ICT TEST DEVICE

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

    HEMOCCULT® ICT TEST DEVICE

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

    HEMOCCULT® ICT TEST DEVICE

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

    HEMOCCULT® ICT TEST DEVICE

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

    HEMOCCULT® ICT TEST DEVICE

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

    HEMOCCULT® ICT TEST DEVICE

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

    SINGLE USE ELECTROSURGICAL KNIFE KD-650

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code KNS·August 11, 2022