BEUDAMED
    9 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.
    Filters Regulation: Us FDA ×

    CATHETER, INTRAVASCULAR OR PERCUTANEOUS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704282917·ISRAEL RETRACTOR 9 1/2" 3 PRONGS

    Symmetry Surgical

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482149393·Allis Grasping Forceps 5.0 mm, 33.0 cm Non-Locking

    AutoDensity

    FDA 510(k)
    FDA Class 2 ·Radiology

    Arthrex RetroFusion Screw

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    IMPELLA 5.5

    FDA Adverse Event
    Injury ·ABIOMED, INC.·Product code OZD·December 26, 2025

    ENDURANT ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code MIH·February 8, 2013

    SWAN-GANZ SYNTHETIC CONTROLCATH THERMODILUTION CATHETERS

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES, PR·Product code DYG·January 6, 2011

    ECHELON LINEAR CUTTER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 22, 2014