BEUDAMED
    32 results · 30ms · Sources: EU EUDAMED, US FDA

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    ULTRA-THIN SDS BALLOON DILATATION CATHETER

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

    ULTRA-THIN SDS BALLOON CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LIT·December 1, 2006

    ULTRA-THIN SDS BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP.·Product code DQY·March 27, 2007

    ULTRA-THIN SDS BALLOON CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code DQY·December 28, 2006

    ULTRA-THIN SDS BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP.·Product code DQY·March 5, 2007

    ULTRA-THIN SDS BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 28, 2006

    ULTRA-THIN SDS BALLOON CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORP.·Product code DQY·April 12, 2007

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776201401·BIMANUAL HANDPIECE IRRIGATING G TITANIUM

    COLOR SPEX

    FDA UDI
    FGX INTERNATIONAL INC.·00193033338643·

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0112090·Tap, Cannulated, 7.5 mm

    COLOR SPEX

    FDA UDI
    FGX INTERNATIONAL INC.·00193033338650·

    COLOR SPEX

    FDA UDI
    FGX INTERNATIONAL INC.·00193033338629·

    COLOR SPEX

    FDA UDI
    FGX INTERNATIONAL INC.·00193033338636·

    NONABSORBABLE POLYPROPYLENE SURGICAL SUTURE

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

    PLAINSENSE WHEELCHAIR

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·July 2, 2019

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code KDJ·March 19, 2013

    ECLIPSE FILTER SYSTEM - FEMORAL

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·February 14, 2011

    CANNULA SET, THREADED, 6MM X 75MM

    FDA Adverse Event
    Malfunction ·CONMED LINVATEC·Product code GEA·March 10, 2008

    VITEK® 2 AST-ST01 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code LON·October 24, 2017