BEUDAMED
    10 results · 25ms · 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 ×

    ACUITY PRO LEAD DELIVERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MODIFICATION TO:RAVEN BACTERIAL SPORE STRIPS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TQ HBA1C GEN3

    FDA 510(k)
    FDA Class 2 ·Hematology

    INTERMATE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code FRN·February 20, 2015

    INTERMATE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code FRN·February 20, 2015

    INTERMATE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code FRN·February 20, 2015

    EPD 60000 RPM

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWE·May 29, 2013

    EASYTRAK 3

    FDA Adverse Event
    Death ·CPI - DEL CARIBE·Product code NIK·October 1, 2014

    EXTENSION SET

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·June 17, 2011

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·February 11, 2025