BEUDAMED
    7 results · 20ms · 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 ×

    ELECTROSURGICAL ELECTRODE

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

    BICONCAVE VITRECTOMY LENS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    FREEMAN TOTAL HIP SYSTEM RIDGED STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    G4 PLATINUM PEDIATRIC CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·June 25, 2014

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code KDJ·January 3, 2013

    ANEURX STENT GRAFT (FLEXIBLE HDM) WITH XPEDIENT

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR·Product code MIH·November 2, 2010

    PHILIPS CPAP DEVICE

    FDA Adverse Event
    Injury ·RESPIRONICS,INC.·Product code BZD·November 8, 2022