BEUDAMED
    6 results · 17ms · 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.

    CATALOGUE NUMBER 321-07/15/50

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    TOUCH 'N HEAT MODEL 5002, MODIFICATION

    FDA 510(k)
    FDA Class 1 ·Dental

    DEKNATEL(TM) PLEUR-EVAC(R) THORACIC CATHETER

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    BOXED INCISOR PLUS BL,(BX6)

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC.·Product code HAB·July 28, 2015

    LAUNCHER 6F GUIDE CATHETER

    FDA Adverse Event
    Injury ·MEDTORNIC, INC·Product code DQY·February 6, 2013

    PELORIS RAPID TISSUE PROCESSOR

    FDA Adverse Event
    Malfunction ·LEICA BIOSYSTEMS MELBOURNE·Product code IEO·December 16, 2010