BEUDAMED
    10 results · 19ms · 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.

    SAS SALOMNELLA 0 GROUP L FACTOR 21 ANTISERUM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Eye Shield

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111147·FOX EYE SHIELD W/ GARTER PED PACK OF 50

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·September 5, 2024

    ACUMED LASER, MODEL 1000

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    ABL90 FLEX PLUS

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    NA

    FDA Adverse Event
    Malfunction ·STERILMED, INC.·Product code NLH·June 24, 2014

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·December 17, 2010

    NUCLEUS CI512 COCHLEAR IMPLANT WITH CONTOUR ADVANCE ELECTRODE

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD·Product code MCM·February 13, 2013

    MONOCRYL UD 27IN USP2-0

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAN·October 25, 2024

    MONOCRYL UD 27IN USP2-0

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAN·October 25, 2024