BEUDAMED
    26 results · 22ms · Sources: EU EUDAMED, US FDA

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    Ortho MI System

    FDA 510(k)
    FDA Class 2 ·Dental

    CUROS PORT PROTECTOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    FHC MICROTARGETING DRIVE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    IOLAB

    FDA Adverse Event
    Injury ·CHIRON·Product code HQL·January 2, 1998

    DALL MILES CABLE

    FDA Adverse Event
    Injury ·HOWMEDICA INC.·Product code JDQ·February 23, 1999

    SILTEX SALINE-FILLED-2800 ROUND

    FDA Adverse Event
    Injury ·MENTOR CORP.·Product code FWM·January 9, 1998

    CRYOVALVE

    FDA Adverse Event
    Injury ·CRYOLIFE, INC.·Product code MIE·October 7, 1998

    PACEMAKER

    FDA Adverse Event
    Injury ·MEDTRONIC·Product code DRO·July 13, 1992

    SHOWER CHAIR

    FDA Adverse Event
    UNKNOWN·Product code FRJ·May 21, 1992

    FLEXI-FLATE SELF CONTAINED PENILE PROSTHESIS

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code FAE·November 20, 1992

    DATASCOPE INTRA-AORTIC BALLOON

    FDA Adverse Event
    Malfunction ·DATASCOPE·Product code DSP·January 15, 1993

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·July 8, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 29, 2014

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    POPULAR PLASTICS·Product code IKX·July 8, 2013

    HARVARD PCA INFUSER

    FDA Adverse Event
    Death ·C.R. BARD, INC.·Product code MEA·September 4, 1992

    PANCREATIC PROVIDER

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES-HOSPITAL PRODUCTS DIVISION·Product code MEA·July 1, 1992

    GROSHONG CATHETER

    FDA Adverse Event
    Injury ·DAVOL PRODUCT·Product code DQT·July 8, 1992

    BI POLAR FEMORAL CUP (43 MILLIMETERS)

    FDA Adverse Event
    Malfunction ·BIO MET·Product code KXA·July 30, 1992

    SIREGRAPH B FOOTBOARD

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SYSTEMS, INC.·Product code KXJ·January 11, 1993

    ELECTRIC DERMATOME HANDPIECE

    FDA Adverse Event
    Injury ·ZIMMER SURGICAL·Product code GFD·June 20, 2013