BEUDAMED
    67 results · 86ms · 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·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

    SOFLEX THREE-PIECE FOLDABLE LENS

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

    VHS LAG SCREW

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

    O.B. APPLICATOR TAMPON

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

    AORTIC HEMODYNAMIC PLUS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.·Product code LWQ·February 26, 1999

    SILTEX LOW BLEED GEL-FILLED MAMMARY PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR·Product code FTR·July 1, 1999

    WALLSTENT ENTERAL PROSTHESIS

    FDA Adverse Event
    Injury ·PLYMOUTH TECHNOLOGY CENTER·Product code MQR·August 3, 1999

    BAXTER LIFESPAN EPTFE VASCULAR GRAFT

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORP.·Product code DSY·August 4, 1999

    AUTO SUTURE ROTICULATOR 55-4.8

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL CORP·Product code GAG·February 3, 1998

    KUGLIN HOOK

    FDA Adverse Event
    Injury ·UNK·Product code HQC·May 27, 1999

    BARD PORT IMPLANT PORT WITH GROSHONG CATHETER

    FDA Adverse Event
    Injury ·C.R. BARD, INC.·Product code LJT·November 22, 1999

    DRAINAGE SET

    FDA Adverse Event
    Injury ·COOK, INC.·Product code FGE·August 13, 1999

    AUTO SUTURE ENDO CLIP 5MM

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL CORP.·Product code GCJ·November 23, 1999

    RESUME TL

    FDA Adverse Event
    Injury ·MEDTRONIC INC.·Product code GZB·April 14, 1999