BEUDAMED
    52 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    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

    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

    SOFTFORM FACIAL IMPLANT

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

    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

    COATED VICRYL (POLYGLACTIN 910) SUTURE

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

    SOFTFORM FACIAL IMPLANT

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

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·September 10, 1999

    AUTO SUTURE PREMIUM MULTIFIRE TA 90-3.5

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL CORP.·Product code GAG·April 9, 1998

    ULTRA-THIN SDS BALLOON CATHETER

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

    LIFEPORT VASCULAR ACCESS SYSTEM

    FDA Adverse Event
    Injury ·HORIZON MEDICAL PRODUCTS, INC.·Product code LJT·October 14, 1999

    HEARTMATE VE LVAS

    FDA Adverse Event
    Injury ·THERMO CARDIOSYSTEMS, INC.·Product code DSQ·March 2, 1999

    BAXTER STRAIGHT CATH KIT

    FDA Adverse Event
    Injury ·ALLEGIANCE HEALTHCARE CORP.·Product code KOD·March 3, 1999

    UNK

    FDA Adverse Event
    Injury ·ALLEGIANCE HEALTHCARE CORP.·Product code KOD·March 3, 1999

    STAR TOTAL ANKLE REPLACEMENT

    FDA Adverse Event
    Injury ·SMALL BONE INNOVATIONS, INC.·Product code NTG·October 22, 2013