BEUDAMED
    212 results · 33ms · Sources: EU EUDAMED, US FDA

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    METRICIDE

    FDA Adverse Event
    METREX RESEARCH CORP.·Product code LRJ·January 5, 1994

    FREESTYLE FREEDOM

    FDA Adverse Event
    Injury ·ABBOTT DIABETES CARE INC·Product code LFR·July 1, 2008

    ONE TOUCH II

    FDA Adverse Event
    Other ·LIFESCAN, INC.·Product code CFR·May 6, 1998

    MALONEY TAPERED MERCURY FILLED

    FDA Adverse Event
    Malfunction ·PILLING CO.·Product code KNQ·June 2, 1999

    PILLING

    FDA Adverse Event
    Injury ·PILLING CO·Product code DWP·April 12, 1999

    LIFELOK

    FDA Adverse Event
    Injury ·PILLING CO.·Product code DXC·August 4, 1994

    HURST BOUGIE OR DILATOR

    FDA Adverse Event
    PILLING CO.·Product code FAT·April 12, 1994

    LEHEY CLAMP

    FDA Adverse Event
    Injury ·PILLING CO·Product code GDJ·October 22, 2002

    ESSURE

    FDA Adverse Event
    Injury ·BAYER·Product code HHS·September 25, 2015

    TROJAN LATEX CONDOM UNSPECIFIED

    FDA Adverse Event
    Malfunction ·CHURCH & DWIGHT CO., INC.·Product code HIS·April 7, 2022

    BAUSCH AND LOMB RENU MOISTURE LOC

    FDA Adverse Event
    Injury ·BAUSCH & LOMB·Product code LPN·April 11, 2006

    MEDICATION CUP

    FDA Adverse Event
    SOLO CUP CO.·Product code KYW·February 23, 1995

    SURGITEK SILICONE BREAST IMPLANT

    FDA Adverse Event
    MEDICAL ENGINEERING CORP.·Product code FTR·June 9, 1994

    POWER PICC SOLO2 CATHETER WITH SHERLOCK 3CG TIP

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS INC.·Product code LJS·January 19, 2015

    ONE TOUCH ULTRA

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·December 13, 2005

    PORT-A-CATH II SYSTEM

    FDA Adverse Event
    Injury ·SIMS DELTEC·Product code LJT·August 11, 2000

    ADKINS STRUTT, 22 CM

    FDA Adverse Event
    Injury ·PILLING INSTRUMENT CO.·Product code KTW·November 28, 1994

    MAHONEY DILATOR

    FDA Adverse Event
    Injury ·PILLING INSTRUMENT CO.·Product code KNQ·December 27, 1996

    KERRISON RONGEUR

    FDA Adverse Event
    Malfunction ·PILLING WECK CO.·Product code HTX·October 31, 1995

    ONE TOUCH ULTRA

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code CFR·February 3, 2004