BEUDAMED
    7 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 ×

    RESPIRATORY SYNCYTIAL VIRUS

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Deltaven Fast Flash

    FDA UDI
    DELTA MED SPA·08032248384361·Safety IV catheter in PUR with closed system, d...

    CMOS Video Nasopharyngoscope System

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    Xenco Medical CancelleX Cervical Interbody System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FLEXI-SEAL CONTROL FMS KIT US

    FDA Adverse Event
    Malfunction ·CONVATEC INC.·Product code KNT·March 25, 2014

    PRIME ZOOM STRETCHER, 30" LITTER

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code INK·October 25, 2012

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·September 21, 2010