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

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    Filters FDA Adverse Event ×

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·November 2, 1999

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·July 9, 1999

    SURGICAL STAINLESS STEEL SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAQ·January 8, 2010

    CENTRAL VENOUS CATHETER

    FDA Adverse Event
    Other ·NEOSTAR MEDICAL TECHNOLOGIES/HORIZON MEDICAL PRODUCTS, INC.·Product code LJT·March 2, 1999

    ANGIO-SEAL

    FDA Adverse Event
    Injury ·THE KENDALL CO.·Product code MGB·March 4, 1999

    CD HORIZON CONICAL CORE SCREW

    FDA Adverse Event
    Injury ·SOFAMOR DANEK EUROPE·Product code HWC·May 11, 1999

    ANGIO-SEAL

    FDA Adverse Event
    Injury ·THE KENDALL CO.·Product code MGB·March 4, 1999

    LP10 VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·December 3, 1999

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·April 19, 2000

    LP10 VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·April 27, 1999

    ASSURANCE 2000 HEART RATE/RESPIRATION MONITOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code FLS·July 28, 1999

    UNKNOWN VESICA PERC STABILIZATIION KIT W/PROTEGEN

    FDA Adverse Event
    Injury ·MICROVASIVE UROLOGY/ A DIVISION OF BOSTON SCIENTIFIC CORP.·Product code FTL·June 16, 2000

    CADENCE V-110C

    FDA Adverse Event
    Injury ·VENTRITEX·Product code LWS·July 9, 1999

    ULTRA-THIN SDS BALLOON CATHETER

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

    CD1700 CS

    FDA Adverse Event
    Other ·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·August 3, 1999

    COATED VICRYL (POLYGLACTIN 910) SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC. SAN ANGELO·Product code GAM·August 2, 1999

    1415939-1999-00013

    FDA Adverse Event
    Other ·December 23, 1999

    ULTRA-THIN SDS BALLOON CATHETER

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

    NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM FOR CHILDREN

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·October 19, 1999

    AUTO SUTURE PREMIUM PLUS CEEA 31MM

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code GAG·April 28, 1998