BEUDAMED
    217 results · 23ms · Sources: EU EUDAMED, US FDA

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    SOFT TISSUE ANCHORING WASHERS

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Latitude™ EV

    FDA UDI
    TORNIER, INC.·00846832002511·Ulnar Stem - Coated

    Tornier Latitude

    FDA UDI
    TORNIER, INC.·00846832014798·HUMERAL BROACH ADAPTER

    Humelock Reversed Shoulder

    FDA UDI
    FX SOLUTIONS·03701037306017·HUMELOCK REVERSED ARCH Ø40

    Intess L

    FDA UDI
    Kalitec Direct LLC·B07312K0100310·Assembly,Caddie, Lumbar Implants, Hinged

    Matira

    FDA UDI
    Kalitec Direct LLC·B073DRK010031·Drill Guide, Straight, Featureless, Amann

    Inseption

    FDA UDI
    Kalitec Direct LLC·B07314K0100310·Assembly, Caddie, ISP Implants, Hinged

    AQUANET, MODEL EC 2000

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

    LENSOCLEAN MULTI-PURPOSE SOLUTION, MODEL 355ML

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    VENTAK PRX

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

    SIMILAR DEVICE BNI75TCDDH, PMA # P030031

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·October 2, 2017

    SIMILAR DEVICE DI7TCBLRT, PMA # P030031

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·February 9, 2015

    VENTAK PRX AUTOMATIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS·Product code LWS·July 8, 1997

    VENTAK PRX AUTOMATIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS·Product code LWS·May 8, 1997

    VENTAK PRX AUTOMATIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS·Product code LWS·May 8, 1997

    VENTAK PRX AUTOMATIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS·Product code LWS·May 8, 1997

    VENTAK PRX AUTOMATIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS·Product code LWS·January 16, 1997

    VENTAK PRX AUTOMATIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS·Product code LWS·January 9, 1997

    VENTAK PRX AUTOMATIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS·Product code LWS·January 9, 1997

    VENTAK PRX AUTOMATIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS·Product code LWS·January 9, 1997