BEUDAMED
    6 results · 18ms · 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.

    CARDISUNY, 501BX

    FDA 510(k)

    MODIFICATION TO: NANOCROSS 0.14 OTW PTA DILATATION CATHETER, MODELS AB14W020210090, AB14W020210150

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SOFTFORM FACIAL IMPLANT

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Injury ·DEXCOM, INC.·Product code MDS·June 27, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·November 17, 2010

    WECK DERMAHOOK 1/2" HOOK 10 PKG/BX 6 HKS/PKG

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code GDG·December 12, 2012