BEUDAMED
    7 results · 29ms · 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.
    Filters Regulation: Us FDA ×

    VYGON XRO VENOUS/ARTERIAL UMBILICAL CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ZI BLOWER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    TOESCO AQUA BLUE LED LIGHT CURING DEVICE

    FDA 510(k)
    FDA Class 2 ·Dental

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    JUNCHENG·Product code ITJ·January 17, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 6, 2014

    ATTAIN OTW

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 13, 2010

    SMR GLENOID BASEPLATE SMALL-R

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·August 26, 2021