BEUDAMED
    66 results · 33ms · Sources: EU EUDAMED, US FDA

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    PERFADEX WITH THAM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    WHITE KNIGHT BLUE, GREEN FACE MASK, (4 MODELS)

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

    MODULAR VALVE HANDLES FOR ADAPTABLE TUBES, MODEL 1298-XX-XX, 1295-XX-XX

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    TRICON/GENESIS KNEE

    FDA Adverse Event
    Injury ·SMITH & NEPHEW INC. ORTHOPAEDICS DIV.·Product code HSH·October 30, 1997

    MOD II UNICOMPARTMENTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC., ORTHOPAEDICS DIV.·Product code HTG·September 25, 1998

    MAXIM PRIMARY TIB. BEAR

    FDA Adverse Event
    Injury ·BIOMET, INC.·Product code HSH·January 8, 2001

    SWEET TIP BIPOLAR LEAD

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS·Product code DXY·September 8, 1997

    BIOMET

    FDA Adverse Event
    Injury ·BIOMET, INC.·Product code JDI·January 2, 1998

    VENTAK P2

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS·Product code LWS·August 5, 1998

    VENTAK AV

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS·Product code LWS·February 8, 1998

    ENDOTAK DOWN-SIZED PLUS

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS·Product code LWS·November 7, 1997

    VENTAK AV AUTOMATIC CARDIOVERTOR DEFIBRILLATOR

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS·Product code LWS·November 7, 1997

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·June 22, 1998

    SKLAR INSTRUMENTS

    FDA Adverse Event
    Injury ·SKLAR INSTRUMENTS·Product code HDF·September 17, 1997

    ABBOTT AXSYM SYSTEM

    FDA Adverse Event
    Other ·ABBOTT MANUFACTURING, INC.·Product code JJE·August 11, 1997

    COATED VICRYL (POLYGLACTIN 910) SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAM·July 13, 2004

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·June 27, 2017

    NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·August 14, 1997

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 23, 2014

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 8, 2024