BEUDAMED
    121 results · 26ms · Sources: EU EUDAMED, US FDA

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    BIOSTINGER MENISCAL REPAIR DEVICE

    FDA Adverse Event
    Other ·LINVATEC CORP.·Product code HWC·August 27, 1999

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·February 28, 2000

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·December 15, 1999

    CRANIOFIX TITANIUM CLAMP STERILE

    FDA Adverse Event
    Injury ·AESCULAP AG & CO. KG·Product code GXR·June 3, 1999

    VASCO TIP BI 9/58

    FDA Adverse Event
    Malfunction ·VASCO MED·Product code DTB·June 16, 1999

    SOFLEX THREE-PIECE FOLDABLE LENS

    FDA Adverse Event
    Injury ·CHIRON VISION CORP.·Product code HQL·April 30, 1999

    GROSHONG 4 FR MIDLINE

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code DQO·March 1, 1999

    B-D 10 ML SYRINGE LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO.·Product code FMI·March 1, 1999

    VHS LAG SCREW

    FDA Adverse Event
    Injury ·BIOMET, INC.·Product code HRS·May 27, 1999

    AUTO SUTURE MULTIFIRE GIA 80-4.8

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP·Product code GAG·May 20, 1998

    O.B. APPLICATOR TAMPON

    FDA Adverse Event
    Injury ·JOHNSON AND JOHNSON, S.A.·Product code HEB·March 29, 1999

    UNK

    FDA Adverse Event
    Other ·SAFESKIN CORP.·Product code LYY·August 19, 1999

    LP10 VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·July 23, 1999

    HAKIM PROGRAMMABLE VALVE WITH PRECHAMBER

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON PROFESSIONAL, INC. MEDOS S.A.·Product code JXG·January 21, 2000

    RADIONICS

    FDA Adverse Event
    Injury ·RADIONICS, INC.·Product code JXG·March 8, 1999

    SILTEX SALINE MAMMARY PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR·Product code FWM·May 11, 1999

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·September 27, 1999

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·February 17, 1999

    AUTO SUTURE PREMIUM SURGICLIP M-9.75

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code GAG·June 19, 1998

    AUTO SUTURE ILA 100 DISPOSABLE LOADING UNIT

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code GAG·May 26, 1998