BEUDAMED
    20 results · 24ms · Sources: EU EUDAMED, US FDA

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    Electronic Pulse Stimulator

    FDA 510(k)
    FDA Class 2 ·Neurology

    POWDER-FREE NITRILE PATIENT EXAMINATION GLOVES, BLUE COLOR

    FDA 510(k)
    FDA Class 1 ·General Hospital

    DHS DISPOSABLE HOOD SYSTEM

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

    SMOOTH LOW BLEED GEL-FILLED MAMMARY PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR·Product code FTR·August 31, 1998

    TSRH SPINAL FIXATION SYSTEM

    FDA Adverse Event
    Injury ·SOFAMOR DANEK MFG·Product code KWP·May 29, 1998

    CD SCREW

    FDA Adverse Event
    Injury ·SOFAMOR DANEK EUROPE·Product code KWP·May 29, 1998

    SIMPLATE II

    FDA Adverse Event
    Injury ·ORGANON TEKNITA CORPORATION·Product code JCA·July 31, 1992

    DOME SUBCUTANEOUS PORT W/GROSHING CATHETER

    FDA Adverse Event
    Malfunction ·DAVOL, INC.·Product code MDX·September 16, 1992

    INTERMEDIATE HI-LO MODEL

    FDA Adverse Event
    Malfunction ·MALLINCKRODT·Product code BSK·July 31, 1992

    ZIMMER AIR DERMATOME HANDPIECE

    FDA Adverse Event
    Injury ·ZIMMER SURGICAL·Product code GFD·July 11, 2013

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·August 17, 2011

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·November 3, 2014

    HEARTSTART XL+ DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·July 3, 2013

    SINGLE VENTRICULAR PASSIVE FIXTURE TIMED LEAD

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DTB·November 20, 1992

    THORACICSILICONE CATHETER

    FDA Adverse Event
    Injury ·AXION TRAUM MEDICAL, INC.·Product code FFA·April 17, 1992

    PCA INFUSER

    FDA Adverse Event
    Malfunction ·IVAC·Product code MEA·March 27, 1993

    UNKNOWN

    FDA Adverse Event
    Injury ·UNKNOWN·Product code FTR·May 22, 1992

    SUPRACONDYLAR PLATE AND SCREWS

    FDA Adverse Event
    Injury ·SYNTHES·Product code JDP·July 10, 1992

    POSEY GERIATRIC CHAIR-Y-SAFETY BELT

    FDA Adverse Event
    Death ·J.T. POSEY COMPANY·Product code FMQ·June 26, 1992

    MONOPOLAR BAYONET COAGULATION FORCEPS

    FDA Adverse Event
    Injury ·WECK·Product code HTD·July 24, 1992